-
Supernumerary chromosomes in six patients.
Clin Genet. 1982 Jun;21(6):397-406
PMID: 6957276
-
An extra idic(15p)(q11) chromosome in Prader-Willi syndrome.
Hum Genet. 1980;55(3):409-11
PMID: 6162774
-
Further studies on the frequency of constitutional chromosome abnormalities in patients with malignant disease.
Eur J Cancer. 1972 Aug;8(4):373-9
PMID: 5073300
-
Cat-eye syndrome, a partial trisomy 22.
Humangenetik. 1972;15(2):150-62
PMID: 5049068
-
The "cat eye syndrome": dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical picture.
Hum Genet. 1981;57(2):148-58
PMID: 6785205
-
New technique for distinguishing between human chromosomes.
Nat New Biol. 1971 Jul 7;232(27):31-2
PMID: 4105244
-
Chromosome surveys in penal institutions and approved schools.
J Med Genet. 1971 Mar;8(1):49-58
PMID: 5098071
-
Leukocytes cultured from small inocula of whole blood and the preparation of metaphase chromosomes by treatment with hypotonic KCl.
Stain Technol. 1965 Nov;40(6):333-8
PMID: 5866557
-
[A small supernumerary metacentric chromosome: interprétation test (author's transl)].
J Genet Hum. 1976 Jun;24(2):81-93
PMID: 965953
-
Two kinships with accessory bisatellited chromosomes.
Ann Genet. 1973 Jun;16(2):101-7
PMID: 4541901
-
Autoradiographic investigations of centric fragments and rings in patients with stigmata of gonadal dysgenesis.
Cytogenetics. 1967;6(3):254-67
PMID: 6040474
-
Cytogenetic and clinical studies in five cases of inv dup(15).
Hum Genet. 1979 Sep;50(3):259-70
PMID: 489010
-
Prader-Willi syndrome and a bisatellited derivative of chromosome 15.
Clin Genet. 1980 Jul;18(1):42-7
PMID: 7418253
-
Small metacentric nonsatellited extra chromosome: report of five mentally retarded individuals and review of literature. Contribution to further delineation of a new syndrome.
Hum Genet. 1978 Oct 19;44(1):59-69
PMID: 711239
-
Cat-eye syndrome with unusual marker chromosome probably not chromosome 22.
Am J Med Genet. 1984 May;18(1):19-24
PMID: 6588751
-
Congenital hypothyroidism in Klinefelter's syndrome.
J Med Genet. 1979 Dec;16(6):439-42
PMID: 537016
-
An improved technique for selective silver staining of nucleolar organizer regions in human chromosomes.
Hum Genet. 1976 Oct 28;34(2):199-206
PMID: 63440
-
Heteromorphic X chromosomes in 46,XX males: evidence for the involvement of X-Y interchange.
Hum Genet. 1979 May 23;49(1):11-31
PMID: 572812
-
The genetic significance of accessory bisatellited marker chromosomes.
Hum Genet. 1983;65(2):155-64
PMID: 6228512
-
Small accessory chromosomes (SAC) and their genotype--phenotype correlation.
J Genet Hum. 1982 Oct;30(3):215-32
PMID: 7153768
-
An extra small metacentric chromosome identified as a deleted chromosome no. 17.
Clin Genet. 1976 May;9(5):454-58
PMID: 1269167
-
Origin of a small metacentric chromosome: familial and cytogenic evidence.
Clin Genet. 1975 Nov;8(5):364-9
PMID: 1204233
-
[Trisomy 21 by translocation (21q,21q) in two sibs of a mother with a supernumerary microchromosome (author's transl)].
Ann Genet. 1981;24(2):117-9
PMID: 6460462
-
B-chromosome systems in flowering plants and animal species.
Int Rev Cytol. 1975;40:1-100
PMID: 1097353
-
Preferential maternal derivation in inv dup(15): analysis of eight new cases.
Hum Genet. 1981;57(4):345-50
PMID: 7286973
-
Chromosome changes in Alzheimer's presenile dementia.
J Med Genet. 1983 Feb;20(1):46-51
PMID: 6842534
-
The aetiology of the cat eye syndrome reconsidered.
J Med Genet. 1981 Apr;18(2):108-18
PMID: 7241528
-
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
-
A simple technique for demonstrating centromeric heterochromatin.
Exp Cell Res. 1972 Nov;75(1):304-6
PMID: 4117921
-
A cytogenetic survey of 11,680 newborn infants.
Ann Hum Genet. 1974 May;37(4):359-76
PMID: 4277977
-
C-bands in seven cases of accessory small chromosomes.
Clin Genet. 1977 Nov;12(5):285-9
PMID: 589849
-
Discovery of an inherited bisatellited metacentric microchromosome in amniotic cell culture.
Clin Genet. 1979 Sep;16(3):183-90
PMID: 90568
-
Mosaic inversion duplication of chromosome 15 without phenotypic effect: occurrence in a father and daughter.
Am J Med Genet. 1984 Mar;17(3):649-54
PMID: 6585144
-
Chromosome survey of new patients admitted to the four maximum security hospitals in the United Kingdom.
Clin Genet. 1976 Apr;9(4):389-98
PMID: 1261079
-
Significance of detection of extra metacentric microchromosome in amniotic cell culture.
J Med Genet. 1978 Apr;15(2):136-42
PMID: 641948
-
Properties and significance of a small marker chromosome in amniotic fluid cells.
Clin Genet. 1980 Oct;18(4):253-6
PMID: 6934054
-
A G-band study of chromosomes in liveborn infants.
Ann Hum Genet. 1980 Jan;43(3):227-39
PMID: 7362200
-
Chromosome abnormalities in human embryos after in vitro fertilization.
Nature. 1983 May 26;303(5915):336-8
PMID: 6855885
-
The origin and behavior of two isodicentric bisatellited chromosomes.
Am J Hum Genet. 1977 May;29(3):294-300
PMID: 868876
-
A cytogenetic study of 1000 spontaneous abortions.
Ann Hum Genet. 1980 Oct;44(Pt 2):151-78
PMID: 7316468
-
Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15.
Hum Genet. 1977 Apr 7;36(1):1-12
PMID: 323137
-
Cytological mapping of human chromosomes: results obtained with quinacrine fluorescence and the acetic-saline-Giemsa techniques.
Chromosoma. 1971;35(3):310-25
PMID: 4109086
-
Chromosome survey of a hospital for the mentally subnormal. 2. Autosome abnormalities.
Clin Genet. 1972;3(4):226-48
PMID: 4262353
-
Cytogenetics and infertility in man. I. Karyotype and seminal analysis: results of a five-year survey of men attending a subfertility clinic.
Ann Hum Genet. 1975 Oct;39(2):231-54
PMID: 1052767
-
Chromosome studies on male patients at a mental subnormality hospital.
Clin Genet. 1971;2(6):338-46
PMID: 5155310
-
Prenatal detection of an accessory chromosome identified as an inversion duplication (15).
Hum Genet. 1981;57(4):357-9
PMID: 7286975
-
Inv dup (15) with mental retardation but few dysmorphic features.
J Med Genet. 1984 Jun;21(3):221-3
PMID: 6748020