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Letter: Possible evidence for Xp plus in and XX Male.
Lancet. 1974 Jun 15;1(7868):1223
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The HLA-dependent expression of testis- organizing H-Y antigen by human male cells.
Cell. 1978 Mar;13(3):509-13
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Multiple congenital defects associated with 45,XO-46,XYg- mosaicism.
Am J Dis Child. 1973 Jul;126(1):75-7
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H-Y antigen in a male with 45, X karyotype.
Lancet. 1978 Aug 5;2(8084):313-4
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Familial occurrence of Noonan syndrome.
Am J Dis Child. 1974 May;127(5):696-8
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Possible evidence of X-Y interchange in an XX male.
Lancet. 1977 Mar 5;1(8010):550
PMID: 65650
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45,XO/46,XYg dic mosaicism in a patient with ambiguous genitalia.
Clin Genet. 1976 Mar;9(3):365-70
PMID: 1261075
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Chromosome banding.
J Histochem Cytochem. 1975 Jul;23(7):461-2
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Giemsa-11 staining of chromosome 1: a newly described heteromorphism.
Science. 1978 Oct 6;202(4363):64-5
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Assignment of the H-Y antigen gene to the short arm of chromosome Y.
J Hered. 1979 Jan-Feb;70(1):78-80
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Familial syndrome of streak gonads and normal male karyotype in five phenotypic females.
N Engl J Med. 1970 Jul 2;283(1):6-11
PMID: 5419329
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A probable partial deletion of the Y chromosome in an intersex patient.
Lancet. 1961 Aug 5;2(7197):294-5
PMID: 13695001
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Mapping the locus of the H-Y antigen.
Cytogenet Cell Genet. 1976;16(1-5):175-7
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Fertile XX- and XY-type females in the wood lemming Myopus schisticolor.
Nature. 1976 May 20;261(5557):225-7
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Isochromosome for long arm of Y chromosome in patient with Turner's syndrome and sex chromosome mosaicism (45,X-46,XYqi).
J Med Genet. 1969 Dec;6(4):422-5
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Confirmation of Y/autosome translocation using recombinant DNA.
Hum Genet. 1979;50(1):39-44
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Lateral asymmetry in human constitutive heterochromatin.
Chromosoma. 1975 Aug 11;51(4):301-10
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A phenotypic male with karyotype 45,X:45,X,ace+(?Yg--).
Humangenetik. 1972;15(4):319-26
PMID: 4634448
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Incidence of chromosome aberrations in a child psychiatric hospital.
Clin Genet. 1974;5(3):205
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Probable long-arm deletion of Y chromosome in boy of short stature.
Lancet. 1973 Mar 17;1(7803):608
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Human Y-chromosome-specific reiterated DNA.
Science. 1976 Mar 19;191(4232):1189-90
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XO and male phenotype.
Am J Dis Child. 1974 Jul;128(1):90-1
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Mapping the locus of the H-Y gene on the human Y chromosome.
Science. 1977 Dec 2;198(4320):940-2
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Y to X translocation in man.
Hum Genet. 1977 Apr 15;36(2):129-41
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Template activity of nuclei from stimulated lymphocytes.
Nature. 1969 Jun 28;222(5200):1247-50
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No evidence for a correlation between behaviour and the size of the Y chromosome.
Clin Genet. 1977 May;11(5):349-58
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The influence of inactive chromosomes on human development. Anomalous sex chromosome complements and the phenotype.
Humangenetik. 1973;17(2):105-36
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Reverse banding in the human Y chromosome.
Lancet. 1973 May 26;1(7813):1178-9
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A case of male Turner's syndrome with XXYY sex chromosome constitution.
Jinrui Idengaku Zasshi. 1975 Sep;20(2):131-9
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Letter: Chromosome constitution 47,XYY in relation to stature.
Humangenetik. 1974;24(4):339
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Genes on the Y chromosome influencing rate of maturation in man: skeletal age studies in children with Klinefelter's (XXY) and Turner's (XO) syndromes.
Lancet. 1959 Aug 22;2(7095):141-4
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Heteromorphic X chromosomes in 46,XX males?
Hum Genet. 1979 Nov;52(2):157-67
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H-Y antigen in human intersexuality.
Clin Genet. 1978 Jul;14(1):31-5
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H-Y gene expression in apparent absence of the long arm of the Y chromosome.
Am J Med Genet. 1979;4(2):135-9
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An XX male: cytogenetic and endocrine studies.
Clin Genet. 1975 Feb;7(2):155-62
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Testis-determining H-Y antigen in XO males of the mole-vole (Ellobius lutescens).
Cell. 1977 Apr;10(4):729-32
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Biological bases of psychological sex differences.
Am J Dis Child. 1978 Feb;132(2):170-7
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Recessive sex-determining genes in human XX male syndrome.
Cell. 1978 Nov;15(3):837-42
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Sex chromosome anomalies detection and fluorescence.
Acta Paediatr Scand. 1973 May;62(3):307-8
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A genetic analysis of the normal body-height growth and dental development in man.
Ann Hum Genet. 1975 Oct;39(2):163-71
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Two functional X chromosomes in human fetal oocytes.
Exp Cell Res. 1973 Dec;82(2):464-6
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Sexual and somatic determinants of the human Y chromosome: studies in a 46,XYp- phenotypic female.
Am J Hum Genet. 1979 Jul;31(4):458-68
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Interrelationships of dental maturity, skeletal maturity, height and weight from age 4 to 14 years.
Growth. 1975 Dec;39(4):453-62
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Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.
Proc Natl Acad Sci U S A. 1977 Mar;74(3):1245-9
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Y ring chromosome associated with gonadoblastoma in situ.
Obstet Gynecol. 1973 Jun;41(6):897-901
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[Translocation of the Y chromosome to an autosome in a boy with hypogonadism (author's transl)].
Hum Genet. 1976 Aug 30;33(3):335-6
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Sex ratios in learning and behavior disorders.
Am J Orthopsychiatry. 1963 Jan;33:92-8
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X-Y chromosomal interchange in the aetiology of true hermaphroditism and of XX Klinefelter's syndrome.
Lancet. 1966 Aug 27;2(7461):475-6
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Compound lateral asymmetry in human chromosome 6:BrdU-dye studies of 6q12-->6q14.
Am J Hum Genet. 1978 Mar;30(2):153-9
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Familial XY gonadal dysgenesis.
J Med Genet. 1970 Jun;7(2):105-11
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Sex-chromosome mosaicism of type XYY/XO.
N Engl J Med. 1962 Apr 5;266:699-702
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Mosaicism in XX males.
Hum Genet. 1978 Nov 24;45(1):103-6
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Heteromorphic X chromosomes in 46,XX males: evidence for the involvement of X-Y interchange.
Hum Genet. 1979 May 23;49(1):11-31
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H-Y antigen and the growth of the dominant gonad.
J Med Genet. 1977 Oct;14(5):335-8
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A LATE-DUPLICATING CHROMOSOME IN SPERMATOGONIAL MITOSIS OF THE MOUSE.
Exp Cell Res. 1965 Jun;38:675-7
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Y to X translocation in a woman with reproductive failure. A new rearrangement.
JAMA. 1973 Oct 29;226(5):544-9
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[A rare structural anomaly of the Y chromosome: Y ring (author's transl)].
Arch Genet (Zur). 1974;47(1):52-9
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Q-banding of human chromosomes after BUdR and BCdR treatment.
Hum Genet. 1976 Mar 12;31(3):309-16
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Location of satellite and homogeneous DNA sequences on human chromosomes.
Nat New Biol. 1971 Oct 27;233(43):268-71
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Male with 45,X karyotype.
Clin Genet. 1977 Aug;12(2):97-100
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Deletion of the long arms of the Y chromosome with normal male development and intelligence.
J Med Genet. 1974 Jun;11(2):208-11
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Definitive evidence for the short arm of the Y chromosome associating with the X chromosome during miosis in the human male.
Nature. 1970 Jun 6;226(5249):959-61
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Radioulnar synostosis, behavioral disturbance, and XYY chromosomes.
J Pediatr. 1969 Jan;74(1):103-6
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Reassessment of presumed Y/22 and Y/15 translocations in man using a new technique.
Cytogenet Cell Genet. 1979;23(1-2):90-4
PMID: 83932
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Sizes of deciduous teeth in 47,XYY males.
Am J Hum Genet. 1977 Sep;29(5):486-9
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Clinical and cytological aspects of sex chromosome activity.
Hereditas. 1977;86(1):63-74
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45,X-46,Xr(Y) in a case of asymmetrical testicular differentiation.
Ann Genet. 1974 Mar;17(1):37-40
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Organization and heterogeneity of sequences within a repeating unit of human Y chromosome deoxyribonucleic acid.
Biochemistry. 1979 Jul 24;18(15):3343-53
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Cytogenetics and sex determination in man and mammals.
J Biosoc Sci Suppl. 1970 May;2:7-30
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Satellite DNA III and alkaline Geimsa staining.
Humangenetik. 1975;26(4):329-33
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Dicentric Y chromosome in mixed gonadal dysgenesis.
J Med Genet. 1975 Jun;12(2):210-2
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Y-21 translocation with gonadal and renal dysgenesis and cardiac rupture.
Am J Dis Child. 1974 Oct;128(4):560-3
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Body height and dental development in patients with Turner's syndrome.
Helv Paediatr Acta. 1974;Suppl 34:33-46
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Immunogenetic aspects of abnormal sexual differentiation.
Cell. 1979 Apr;16(4):691-5
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Cytogenetics of Saanen goats showing abnormal development of the reproductive tract associated with the dominant gene for polledness.
Cytogenetics. 1969;8(1):51-67
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Restriction and modification in B. subtilis. Nucleotide sequence recognised by restriction endonuclease R. Bsu R from strain R.
Mol Gen Genet. 1975 Dec 30;143(1):25-33
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The early childhood development of 17 boys with sex chromosome anomalies: a prospective study.
Pediatrics. 1977 Apr;59(4):574-83
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Major regulatory genes for mammalian sexual development.
Cell. 1976 Mar;7(3):315-21
PMID: 181141
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Mapping the locus of the H-Y antigen.
Birth Defects Orig Artic Ser. 1976;12(7):175-7
PMID: 1024610
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KARYOTYPE-PHENOTYPE CORRELATIONS IN GONADAL DYSGENESIS AND THEIR BEARING ON THE PATHOGENESIS OF MALFORMATIONS.
J Med Genet. 1965 Jun;2(2):142-55
PMID: 14295659
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Repeated sequence specific to human males.
Nature. 1976 Jul 15;262(5565):182-6
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DIPI and DAPI: fluorescence banding with only negliglible fading.
Hum Genet. 1977 Apr 15;36(2):167-72
PMID: 67075
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Genome complexity and in vivo transcription in human leukemic leukocytes.
Acta Haematol. 1975;54(4):227-33
PMID: 811036
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Direct activation of DNA template in lymphocyte nuclei treated with phytohemagglutinin.
Biochem Biophys Res Commun. 1972 Mar 24;46(6):2067-74
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Absence of H-Y antigen in XY females with dysgenetic gonads.
Nature. 1978 Nov 9;276(5684):180-1
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Variant of the fluorescence pattern in an abnormal human Y chromosome.
Nature. 1971 Dec 10;234(5328):348
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X/XYq - mosaicism and mixed gonadal dysgenesis.
J Med Genet. 1977 Aug;14(4):262-5
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Chromosome studies on testicular cells from 50 subfertile men.
Lancet. 1966 Jul 9;2(7454):69-71
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A dicentric Y chromosome without evidence of sex chromosomal mosaicism, 46,XYqdic, in a patient with features of Turner's syndrome.
J Med Genet. 1972 Mar;9(1):96-100
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A patient with a dicentric Y chromosome.
Clin Genet. 1974;6(4):326-31
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[Phytohemagglutinin-induced increase of euchromatin contents in human lymphocytes].
Res Exp Med (Berl). 1974;164(1):63-76
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Differential spiralization along mammalian mitotic chromosomes. II. 5-bromodeoxyuridine and 5-bromodeoxycytidine-revealed differentiation in human chromosomes.
Chromosoma. 1974 Jan 29;44(4):343-59
PMID: 4134865
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Oestrogen content of the embryonic rabbit ovary.
Nature. 1978 Jul 13;274(5667):172-3
PMID: 662014
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Structural abnormalities of the Y chromosome in man.
Nature. 1966 Apr 23;210(5034):352-4
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Meiotic studies on a subfertile patient with a ring Y chromosome.
Cytogenetics. 1971;10(4):295-304
PMID: 5127018
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Localisation of a male-specific DNA fragment to a sub-region of the human Y chromosome.
Nature. 1978 Mar 23;272(5651):324-8
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[Aberrations in the structure of the X chromosome in women].
Rev Fr Gynecol Obstet. 1973 Nov;68(11):665-72
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Communications and commentaries: A 46,XYq- male with aspermia.
Fertil Steril. 1973 Oct;24(10):811-3
PMID: 4742003
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Expression of the mammalian X chromosome before and after fertilization.
Science. 1972 Mar 31;175(4029):1467-8
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Fractions of HeLa DNA differing in their content of guanine+cytosine.
J Mol Biol. 1969 Dec 14;46(2):305-12
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Gonadal dysgenesis in two siblings.
Am J Obstet Gynecol. 1976 Jan 15;124(2):208-9
PMID: 1247056
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Unstable ring Y chromosome in an aspermic male.
Hum Genet. 1979 Apr 5;47(3):227-31
PMID: 457111
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Four new cases of Dicentric Y chromosomes.
Hum Genet. 1977 May 10;36(3):249-60
PMID: 852871
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The 47,XYY male, Y chromosome, and tooth size.
Am J Hum Genet. 1975 Jan;27(1):53-61
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45,X-45,X, ace(?Yp)plus-46,X,r(Y) in a phenotypically normal newborn male.
Humangenetik. 1974 May 17;22(2):177-80
PMID: 4135787
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Length of the Y chromosome and antisocial behaviour?
Humangenetik. 1974 Apr 24;22(1):67-9
PMID: 4837291
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Gonadal dysgenesis in individuals with apparently normal chromosomal complements: tabulation of cases and compilation of genetic data.
Birth Defects Orig Artic Ser. 1971 May;7(6):215-28
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Analytic review: nature and origin of males with XX sex chromosomes.
Am J Hum Genet. 1972 Jan;24(1):71-105
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Cytogenetic studies in primary amenorrhoea.
Lancet. 1961 Jun 3;1(7188):1183-9
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The XXXXY sex chromosome abnormality.
Arch Dis Child. 1966 Feb;41(215):82-6
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Length of Y chromosome and activity in boys.
Clin Genet. 1975 Oct;8(4):291-6
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[Extended hypothesis of mosaicism as explanation for XX-men].
Humangenetik. 1974 Jul 15;23(2):161-2
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The sex chromosomes of the Chinese hamster: constitutive heterochromatin deficient in repetitive DNA sequences.
Cytogenet Cell Genet. 1974;13(3):268-74
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Cytogenetical and clinical investigations in four subjects with anomalies of sexual development.
Science. 1967 Jan 13;29(3):281-304
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Pure gonadal dysgenesis (type XX). Report on a family with four affected sibs.
Hum Genet. 1977 Jun 10;37(1):117-20
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Studies on the male meiosis of Ellobius lutescens Th.
Cytogenetics. 1968;7(4):241-8
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Ring Y chromosome without mosaicism.
Birth Defects Orig Artic Ser. 1976;12(5):105-12
PMID: 953209
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Translocations causing non-fluorescent Y chromosomes in human XO/XY mosaics.
Hereditas. 1971;68(2):317-24
PMID: 4142012
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Trimethylaminuria and inherited Noonan's syndrome.
Lancet. 1973 Feb 10;1(7798):320-1
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Length of the Y chromosome in criminal males.
Clin Genet. 1972;3(4):281-5
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X-short arm deletion gonadal dysgenesis in two siblings due to unique translocation (Xp-;16p+).
Clin Genet. 1976 Oct;10(4):202-7
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A case of ring Y chromosome.
Hum Genet. 1978 May 16;42(1):89-91
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Modality and sex differences in recall and recognition memory.
Child Dev. 1974 Mar;45(1):228-31
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A strongly fluorescing abnormal chromosome in a malformed child.
Humangenetik. 1971;12(1):64-6
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Satellite DNA.
J Med Genet. 1973 Sep;10 (3):273-81
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Serologic detection of a y-linked gene in xx males and xx true hermaphrodites.
N Engl J Med. 1976 Sep 30;295(14):750-4
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Isolabeling of the long arm of the human Y chromosome demonstrated by the FPG technique.
Chromosoma. 1978 Oct 20;69(1):113-20
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The location of four human satellite DNAs on human chromosomes.
Exp Cell Res. 1975 Apr;92(1):148-58
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XO-XY mosaicism and nonfluorescent Y chromosome.
Obstet Gynecol. 1973 Sep;42(3):421-8
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Minute Y chromosome.
Ann Genet. 1971 Jun;14(2):145-8
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Letter: X long-arm deletion with features of Turner's syndrome.
Lancet. 1974 Aug 17;2(7877):403-4
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Am J Surg. 1964 Sep;108:370-9
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Xq- Turner's syndrome: reconsideration of hypothesis that Xp- causes somatic features in Turner's syndrome.
J Med Genet. 1970 Mar;7(1):1-4
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Isochromosome for the short arm of X, a human 46, XXpi syndrome.
Ann Hum Genet. 1972 Jul;36(1):79-87
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Isochromosome Y (46,X,i(Yq)) and female phenotype.
Clin Genet. 1973;4(5):410-4
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Staining of some specific regions of human chromosomes, particularly the secondary constriction of No. 9.
Nat New Biol. 1972 Jul 26;238(82):122-4
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A case of quintuple-X syndrome (49,XXXXX).
J Ment Defic Res. 1970 Dec;14(4):305-11
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A boy with 47,X,del(X)(p11leads to q13:q21leads to q24),del(Y)(q11):reexamination of a case previously described as 47,XX,?Yq-.
Hum Genet. 1976 Feb 29;31(2):227-30
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Genetic basis of XX male syndrome and XX true hermaphroditism: evidence in the dog.
Science. 1978 Aug 18;201(4356):644-6
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XXY cells in a predominantly XX human male: evidence for cell selection.
Pediatrics. 1966 Dec;38(6):982-5
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Binding studies of H-Y antigen in rat tissues: indications for a gonad-specific receptor.
Hum Genet. 1978 Aug 31;43(2):151-7
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X-Y translocation in a retarded phenotypic male. Clinical, cytogenetic, biochemical, and serogenetic studies.
J Med Genet. 1978 Dec;15(6):466-74
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[45,X/46,SYq dic-Sexchromosome mosaic].
Humangenetik. 1975;27(2):81-90
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[True hermaphroditism and "XX boy" in a sibship].
Rev Eur Etud Clin Biol. 1970 Mar;15(3):330-3
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Nullisomy for the distal portion of Xp in a male child with a X/Y translocation.
Hum Genet. 1977 Dec 23;39(3):277-81
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Structural aberrations of the Y chromosome and the corresponding phenotype. Report of a case with the karotype 45,X-46,X,i(Yp).
Humangenetik. 1973;19(1):57-66
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Possible role for H--Y antigen in the primary determination of sex.
Nature. 1975 Sep 18;257(5523):235-6
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Effects of distamycin A on human leukocytes in vitro.
Cytogenet Cell Genet. 1979;23(1-2):103-7
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Early development of children with abnormalities of the sex chromosomes: a prospective study.
Pediatrics. 1974 Aug;54(2):208-12
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Evolution of X-chromosome inactivation in mammals.
Nature. 1974 Aug 23;250(5468):651-3
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45,X/47,XYY mosaicism.
J Med Genet. 1977 Jun;14(3):218-21
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H-Y antigen in trans-sexuality.
Lancet. 1979 Nov 24;2(8152):1137-8
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Modification of DAPI banding on human chromosomes by prestaining with a DNA-binding oligopeptide antibiotic, distamycin A.
Exp Cell Res. 1978 Feb;111(2):327-32
PMID: 75107
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Evolutionary conservation of H-Y ('male') antigen.
Nature. 1975 Mar 20;254(5497):270-2
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BSu restriction of DNA from cases exhibiting sex-chromosome abnormalities.
Cytogenet Cell Genet. 1978;20(1-6):59-69
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[Dicentric Y chromosome in a male pseudohermaphrodite 45,X/46,X, dic (Y)/47, XYY].
Ann Genet. 1977 Sep;20(3):185-9
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Localization of male determining factor on short arm of Y chromosome. Case report of a baby with 46, x, t (Yp+;14q-).
Clin Genet. 1972;3(5):381-7
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Ring Y chromosome: 45,X/46,Xr(Y) chromosome mosaicism in a phenotypically normal male with azoospermia.
Hum Genet. 1976 Sep 10;34(1):99-102
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Clinical, pathologic, and genetic findings in a case of 46,XY pure gonadal dysgenesis (Swyer's syndrome). II. Presence of H-Y antigen.
Am J Obstet Gynecol. 1977 Apr 15;127(8):829-31
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Dicentric Yp chromosome in a patient with the gonadal dysgenesis and gonadoblastoma.
Humangenetik. 1975;27(3):251-3
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5-Methylcytosine localised in mammalian constitutive heterochromatin.
Nature. 1974 Oct 18;251(5476):636-7
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Isochromosome Yq in a woman with atypical Turner's syndrome.
Hum Genet. 1977 Aug 31;38(1):49-55
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Mixed gonadal dysgenesis with Turner phenotype and XO-XYq- mosaicism.
Jinrui Idengaku Zasshi. 1970 Sep;15(2):103-13
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Lateral asymmetry in the fluorescence of human Y chromosomes stained with 33 258 Hoechst.
Exp Cell Res. 1974 Aug;87(2):425-9
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Direct familial transmission of the Turner phenotype.
Am J Dis Child. 1968 Oct;116(4):343-50
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Familial XX true hermaphroditism and the H-Y antigen.
Hum Genet. 1979 Apr 17;48(1):45-52
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Presumptive Y/D translocation in mixed gonadal dysgenesis.
J Med Genet. 1967 Mar;4(1):36-40
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Expression of H-Y antigen in human males with two Y chromosomes.
N Engl J Med. 1975 Nov 20;293(21):1070-2
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[Antisocial behaviour and variations in length of Y chromosome (author's transl)].
Hum Genet. 1976 Apr 15;32(1):77-80
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Chromosome aberrations in XO-XY mosaic individuals and their fathers.
Am J Obstet Gynecol. 1967 Dec 15;99(8):1056-66
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Somatic stigmata of Turner's syndrome in a patient with 46,XXq-.
J Med Genet. 1971 Sep;8(3):358-63
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Chromosome measurements on an XXp+ male.
Hum Genet. 1976 May 19;32(2):141-2
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Sexual dimorphism and homosexual gender identity.
Psychol Bull. 1970 Dec;74(6):425-40
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H-Y antigen: behavior and function.
Science. 1977 Mar 11;195(4282):956-60
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Human Y chromosomes with two fluorescing bands after staining with quinacrine derivates.
Humangenetik. 1971;13(3):238-40
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Localization of heterochromatin in human chromosomes.
Cytogenetics. 1971;10(2):81-6
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Cytological differentiation of constitutive heterochromatin.
Chromosoma. 1974;48(4):391-403
PMID: 4141300
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Demonstration of two different regions of lateral asymmetry in human Y chromosomes.
Hum Genet. 1979 Oct 2;51(3):247-52
PMID: 92451
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A comparison of constitutive heterochromatin staining methods in two cases of familial heterochromatin deficiencies.
Hum Genet. 1979 Nov 1;52(1):133-8
PMID: 527974
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Permanent tooth sizes in 46,XX-males.
Ann Hum Genet. 1979 Oct;43(2):97-102
PMID: 575031
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Sex-reversed mice: XX and XO males.
Cytogenetics. 1971;10(5):318-37
PMID: 5156366
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Recessive male-determining genes.
Cell. 1978 Sep;15(1):279-81
PMID: 699047
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Mammalian oocytes: X chromosome activity.
Science. 1969 Mar 7;163(3871):1078-9
PMID: 5764873
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Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm.
Hum Genet. 1976 Oct 28;34(2):119-24
PMID: 1002136
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XYY genotype. Report of a case in a male.
N Engl J Med. 1963 Mar 14;268:585-9
PMID: 13991404
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Fluorescence and autoradiographic studies in patients with Turner's syndrome and 46,XXp- and 46,XXq- karyotypes.
J Med Genet. 1973 Dec;10(4):350-5
PMID: 4129970
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Ontogeny of X-chromosome inactivation in the female germ line.
Exp Cell Res. 1975 Mar 15;91(2):454-7
PMID: 1126394
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Familial true hermaphrodism in three siblings: clinical, cytogenetic, histological and hormonal studies.
Humangenetik. 1975 Sep 10;29(2):99-109
PMID: 1236834
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Nonmosaic 46,X,r(Y) karyotype with female phenotype.
Hum Genet. 1977 Oct 14;38(3):351-6
PMID: 914284
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Timing of sex chromosome replication in somatic and germ-line cells of the mouse and the rat.
Cytogenetics. 1967;6(1):51-66
PMID: 6040471
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Three dicentric Y chromosomes.
Ann Hum Genet. 1970 Jul;34(1):39-50
PMID: 5529233
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XY gonadal dysgenesis and the H-Y antigen. Report on 12 cases.
Hum Genet. 1979 Apr 5;47(3):269-77
PMID: 110669
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The xyy chromosome male--or syndrome?
Prog Med Genet. 1974;10:135-222
PMID: 4283414
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Lateral asymmetry in human constitutive heterochromatin: frequency and inheritance.
Am J Hum Genet. 1978 Mar;30(2):144-52
PMID: 566032
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The magnitude and implications of the relationship between tooth size and body size.
Arch Oral Biol. 1968 Jan;13(1):129-31
PMID: 5237551
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Abnormalities of human sex chromosomes. I. A ring Y without mosaiciam.
Ann Genet. 1973 Dec;16(4):225-31
PMID: 4544085
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Two XX males in one family and additional observations bearing on the etiology of XX males.
Clin Genet. 1977 Feb;11(2):91-106
PMID: 837567
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Serological evidence for H-Y antigen in Sxr, XX sex-reversal phenotypic males.
Nature. 1977 Jan 20;265(5591):255-7
PMID: 834270
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Yq deletion, aspermia, and short stature.
Hum Genet. 1977 Nov 2;39(1):117-22
PMID: 924439
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Lateral asymmetry of constitutive heterochromatin in human chromosomes.
Hum Genet. 1979 Nov 1;52(1):79-84
PMID: 527977
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Reverse fluorescent chromosome banding with chromomycin and DAPI.
Chromosoma. 1976 Nov 29;58(4):307-24
PMID: 137107
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Y-chromosomal genes in a phenotypic male with a 46XX karyotype.
JAMA. 1976 Nov 29;236(22):2505-8
PMID: 1036513
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Familial XY gonadal dysgenesis.
N Engl J Med. 1968 Mar 28;278(13):695-700
PMID: 4295620
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Mithramycin and DIPI: a pair of fluorochromes specific for GC-and AT-rich DNA respectively.
Hum Genet. 1977 May 10;36(3):299-305
PMID: 67077
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TWO XY SIBLINGS WITH GONADAL DYSGENESIS AND A FEMALE PHENOTYPE.
N Engl J Med. 1965 May 27;272:1083-8
PMID: 14281549
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Non-fluorescent Y-chromosome.
Helv Paediatr Acta. 1974 Nov;29(5):447-56
PMID: 4141700
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Evidence for two functional X chromosomes in human oocytes.
Cell Differ. 1972 Oct;1(4):215-8
PMID: 4670884
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Women heterozygous for deficiency of the (p21 leads to pter) region of the X chromosome are fertile.
Hum Genet. 1977 Dec 23;39(3):283-92
PMID: 598836
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Noonan's syndrome. IQ and specific disabilities.
Am J Dis Child. 1979 Aug;133(8):846-50
PMID: 463839
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GONADOBLASTOMA ASSOCIATED WITH PURE GONADAL DYSGENESIS IN MONOZYGOUS TWINS.
J Pediatr. 1964 May;64:740-5
PMID: 14149008
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A new case of XX-male (XX/XXY mosaic).
Hum Genet. 1977 Nov 2;39(1):131-7
PMID: 562834
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X chromosome expression during oogenesis in the mouse.
Dev Biol. 1975 Aug;45(2):366-8
PMID: 1193304
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C-heteromorphism in chromosome no. 6.
Clin Genet. 1979 Oct;16(4):295
PMID: 519899
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A theory explaining the abnormality in 45,X/46,XY mosaicism with non-fluorescent Y chromosome. presentation of three cases.
Ann Genet. 1978 Mar;21(1):5-11
PMID: 308343
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The identification of a repeated DNA sequence involved in the karyotype polymorphism of the human Y chromosome.
Cytogenet Cell Genet. 1978;21(1-2):19-32
PMID: 648195
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Sex determination and gonadal differentiation in man. A unifying concept of normal and abnormal sex development.
Clin Genet. 1971;2(6):379-86
PMID: 5155315
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Presence of brightly fluorescent material in testes of XX males.
J Med Genet. 1973 Jun;10(2):170-4
PMID: 4714585
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Three cases of sex chromosome mosaicism with a nonfluorescent Y.
Hum Genet. 1979 Feb 15;46(3):295-304
PMID: 437772
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The original function of MHC antigens as the general plasma membrane anchorage site of organogenesis-directing proteins.
Immunol Rev. 1977 Jan;33:59-69
PMID: 66186
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Letter: Y-to-X translocation in a girl.
Lancet. 1974 Jan 12;1(7846):68-9
PMID: 4128861
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Influence of temperature on the detectibility and chromosomal distribution of specific DNA sequences by in situ hybridisation.
Chromosoma. 1975 Dec 29;53(4):345-59
PMID: 1212901
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X"Y"-XO MOSAICISM IN A PHENOTYPIC INTERSEX; REPORT OF A CASE.
Am J Clin Pathol. 1965 Mar;43:251-5
PMID: 14270968
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The length of the Y-chromosomes in men examined by forensic psychiatrists.
Hum Genet. 1977 Nov 2;39(1):1-5
PMID: 924436
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Twins discordant for 46,XX gonadal dysgenesis.
Fertil Steril. 1977 Mar;28(3):251-2
PMID: 557003
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X;Y translocation in an adolescent mentally normal phenotypic male with features of hypogonadism.
J Med Genet. 1980 Dec;17(6):437-43
PMID: 6937619
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Genetically determined sex-reversal in 46,XY humans.
Science. 1978 Oct 6;202(4363):53-6
PMID: 567843
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Noonan's syndrome (XX and XY Turner phenotype) in three generations of a family.
J Pediatr. 1972 Jan;80(1):110-4
PMID: 5016336