Home LiteratureArticle Details
PMID: 4865216 Published · ppublish ger Journal Article Review

[On the problem of assigning genes to definite human autosomes with the aid of chromosome aberrations].

Zur frage der Zuordnung von Genen zu bestimmten Autosomen des Menschen mit Hilfe von Chromosomenaberrationen.

Humangenetik ·Vol. 4 ·No. 2 ·1967-00-00 ·Pages 85-103

Bender K, Ritter H, Wolf U

Abstract

暂无摘要

MeSH Terms
Chromosome Aberrations Chromosome Disorders Chromosome Mapping Humans Trisomy
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Bender K
Ritter H
Wolf U
References (75)
75 references, click to expand
  1. [PARTIAL DELETION OF THE LONG ARMS OF THE CHROMOSOME 18].
    Pathol Biol. 1964 May;12:579-82 PMID: 14180960
  2. PHENOTYPIC SHIFTS IN TRISOMY.
    Am J Hum Genet. 1965 Mar;17:111-24 PMID: 14262129
  3. The leucocyte alkaline phosphatase in mongolism.
    Lancet. 1962 Sep 8;2(7254):486-7 PMID: 13922647
  4. [Studies on the activity of galactokinase in the blood of normal persons and of patients with GDo trisomy].
    Humangenetik. 1965;1(3):279-88 PMID: 4223835
  5. THE "CAT CRY" SYNDROME.
    Am J Dis Child. 1964 Nov;108:538-42 PMID: 14209690
  6. [Genetic and clinical study of a family of 7 children in which 3 persons have "crying cat syndrome"].
    Ann Genet. 1966 Sep;9(3):113-22 PMID: 5298289
  7. FAMILIAL SHORT ARM DEFICIENCY OF CHROMOSOME 18 CONCOMITANT WITH ARHINENCEPHALY AND ALOPECIA CONGENITA.
    Am J Hum Genet. 1965 Sep;17:410-9 PMID: 14334740
  8. [FAMILIAL AND ANEUPLOID MARKER CHROMOSOMES. POSSIBLE ROLE OF CHROMOSOME INTERACTION].
    Ann Genet. 1964;7:76-83 PMID: 14249002
  9. "CRI DU CHAT" SYNDROME. A NEW CLINICAL AND CYTOGENETIC ENTITY.
    Lancet. 1965 Jan 2;1(7375):23-5 PMID: 14246676
  10. GALACTOSAEMIA LOCUS AND THE DOWN'S SYNDROME CHROMOSOME.
    Lancet. 1963 Oct 5;2(7310):700-3 PMID: 14057154
  11. Alkaline-phosphatase activity of polymorphs in mongolism.
    Lancet. 1962 Dec 22;2(7269):1302-5 PMID: 14032857
  12. [PARTIAL MONOSOMY FOR A SMALL ACROCENTRIC CHROMOSOME].
    C R Hebd Seances Acad Sci. 1964 Nov 30;259:4187-90 PMID: 14260664
  13. ENHANCEMENT OF ERYTHROCYTE-GALACTOKINASE ACTIVITY IN LANGDON-DOWN TRISOMY.
    Lancet. 1965 Mar 6;1(7384):553 PMID: 14251534
  14. Partial-trisomy syndromes. II. An insertion as cause of the OFD syndrome in mother and daughter.
    Chromosoma. 1961;12:573-84 PMID: 14484286
  15. [Study of somatic chromosomes from 9 mongoloid children].
    C R Hebd Seances Acad Sci. 1959 Mar 16;248(11):1721-2 PMID: 13639368
  16. A new trisomic syndrome.
    Lancet. 1960 Apr 9;1(7128):787-90 PMID: 13819419
  17. CHROMOSOME STUDIES DURING EARLY AND TERMINAL CHRONIC MYELOID LEUKAEMIA.
    Br Med J. 1964 Apr 18;1(5389):1010-4 PMID: 14113474
  18. AUTOSOMALLY DETERMINED POLYMORPHISM OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE IN PEROMYSCUS.
    Science. 1965 May 21;148(3673):1099-100 PMID: 14289612
  19. [5-21-22 translocation and the crying cat syndrome].
    Ann Genet. 1965;8(1):31-8 PMID: 5294631
  20. The leucocyte count in children with mongolism.
    J Ment Sci. 1958 Apr;104(435):457-60 PMID: 13564152
  21. A possible specific chromosome abnormality in human chronic myeloid leukaemia.
    Nature. 1960 Dec 31;188:1165-6 PMID: 13685929
  22. The chromosomes of man.
    Nature. 1956 Nov 10;178(4541):1020-3 PMID: 13378517
  23. MEASUREMENTS OF LIKENESS IN RELATIVES OF TRISOMICS.
    Ann Hum Genet. 1963 Nov;27:183-7 PMID: 14081489
  24. MULTIPLE FORMS OF ENZYMES: TISSUE, ONTOGENETIC, AND SPECIES SPECIFIC PATTERNS.
    Proc Natl Acad Sci U S A. 1959 May;45(5):753-63 PMID: 16590440
  25. [Partial deletion of the long arm of chromosome 18. Individualization of a new morbid state].
    Ann Genet. 1966;9(1):32-8 PMID: 5295700
  26. LE CRI DU CHAT (CRYING CAT) SYNDROME.
    Am J Dis Child. 1964 Nov;108:533-7 PMID: 14209689
  27. [Deletion of the short arms of chromosome No. 18].
    Humangenetik. 1966;2(2):178-85 PMID: 5915640
  28. Blood-group gene localization through a study of mongolism.
    Ann Hum Genet. 1966 Jul;30(1):49-67 PMID: 4225588
  29. SPECIFICITY OF THE PHILADELPHIA CHROMOSOME; CYTOGENIC STUDIES IN CASES OF CHRONIC MYELOCYTIC LEUKEMIA AND MYELOID METAPLASIA.
    Ann Intern Med. 1964 Oct;61:609-24 PMID: 14217124
  30. Completeness of catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes.
    Am J Med Genet. 1992 Jun 1;43(3):606-8 PMID: 1605257
  31. Genetics of fourteen marker systems: associations and linkage relations.
    Acta Genet Stat Med. 1966;16(1):1-58 PMID: 4955839
  32. [FACTOR MAP OUTLINE OF THE X CHROMOSOME].
    Ann Genet. 1964;7:101-5 PMID: 14248997
  33. ABO FREQUENCIES IN MONGOLS.
    Ann Hum Genet. 1964 Jun;27:405-12 PMID: 14175204
  34. [Deletion of the short arm of chromosome 18].
    Ann Genet. 1966;9(1):19-26 PMID: 5295699
  35. Electrophoretic variation in enzymes.
    Science. 1965 Aug 27;149(3687):936-43 PMID: 5318249
  36. DELETION OF THE SHORT ARM OF CHROMOSOME 18.
    Cytogenetics. 1964;3:201-6 PMID: 14227324
  37. STUDIES OF THE PHILADELPHIA CHROMOSOME IN PATIENTS WITH CHRONIC MYELOGENOUS LEUKEMIA.
    Ann N Y Acad Sci. 1964 Feb 28;113:1073-80 PMID: 14120508
  38. [On a case of partial deletion of the short arm of chromosome 18, resulting in a familial 18c-17 translocation].
    Ann Genet. 1966;9(1):27-31 PMID: 5295911
  39. The Duffy blood groups of New York negroes: the phenotype Fy (a-b-).
    Br J Haematol. 1955 Oct;1(4):370-4 PMID: 13269673
  40. Multiple molecular forms of leucine aminopeptidase in man.
    Acta Genet Stat Med. 1966;16(3):223-30 PMID: 5953709
  41. ABO BLOOD GROUPS OF MONGOLS.
    Can Med Assoc J. 1963 Oct 26;89:906 PMID: 14069621
  42. HUMAN RED-CELL PHOSPHOGLUCONATE DEHYDROGENASES.
    Nature. 1963 Nov 30;200:890-1 PMID: 14096069
  43. Bivalent alleles.
    Am J Hum Genet. 1966 May;18(3):233-42 PMID: 5944417
  44. PARTIAL DELETION OF SHORT ARMS OF CHROMOSOME NO. 5. REPORT OF A CASE IN A FRATERNAL TWIN.
    Am J Dis Child. 1965 Jan;109:85-9 PMID: 14218865
  45. ABO frequencies in mongolism.
    Ann Hum Genet. 1966 Jul;30(1):43-8 PMID: 4225587
  46. [3 CASES OF PARTIAL DELETION OF THE SHORT ARM OF A 5 CHROMOSOME].
    C R Hebd Seances Acad Sci. 1963 Nov 18;257:3098-102 PMID: 14095841
  47. [PARTIAL DELETION OF THE SHORT ARM OF CHROMOSOME 5. INDIVIDUALIZATION OF A NEW MORBID STATE].
    Sem Hop. 1964 Apr 14;40:1069-79 PMID: 14144301
  48. Hexose-6-phosphate dehydrogenase found in human liver.
    Science. 1966 Aug 26;153(3739):1015-6 PMID: 5917551
  49. LEUCOCYTE ALKALINE PHOSPHATASE IN KLINEFELTER'S SYNDROME.
    J Med Genet. 1965 Jun;2(2):112-5 PMID: 14295652
  50. Zone electrophoresis in starch gels: group variations in the serum proteins of normal human adults.
    Biochem J. 1955 Dec;61(4):629-41 PMID: 13276348
  51. Further studies on the genetics of placental alkaline phosphatase.
    Ann Hum Genet. 1967 Jan;30(3):219-32 PMID: 6067798
  52. Catalase Hybrid Enzymes in Maize.
    Science. 1964 Nov 27;146(3648):1174-5 PMID: 17832245
  53. [Chromosomal studies in chronic myeloic leukemia].
    Klin Wochenschr. 1966 Jan 1;44(1):12-9 PMID: 5234187
  54. [To the formal genetics of the Duffy system. Investigation of 247 families].
    Humangenetik. 1967;4(1):59-61 PMID: 6081913
  55. ACID-PHOSPHATASE ACTIVITY IN PARTIAL TRANSLOCATION-TRISOMY.
    Lancet. 1965 Apr 3;1(7388):768 PMID: 14255264
  56. Anti-mongolism. Studies in an infant with a partial monosomy of the 21 chromosome.
    Lancet. 1966 Feb 19;1(7434):394-7 PMID: 4159779
  57. STUDIES ON GALACTOSE OXIDATION IN DOWN'S SYNDROME.
    N Engl J Med. 1964 May 21;270:1085-8 PMID: 14121488
  58. [Deficiency on the short arms of a chromosome No. 4].
    Humangenetik. 1965;1(5):397-413 PMID: 5868696
  59. Multiple congenital anomaly caused by an extra autosome.
    Lancet. 1960 Apr 9;1(7128):790-3 PMID: 14430807
  60. GENETIC STUDIES ON MUTANT ENZYMES IN MAIZE: SYNTHESIS OF HYBRID ENZYMES BY HETEROZYGOTES.
    Proc Natl Acad Sci U S A. 1960 Sep;46(9):1210-5 PMID: 16590735
  61. [Deletion of the short arm of a 13-15 chromosome, hypertelorism and Hp0 haptoglobin phenotype in the same family].
    Ann Genet. 1966 Jun;9(2):80-5 PMID: 5296303
  62. [Clinical and genetic studies of a patient with crying cat syndrome].
    Dtsch Med Wochenschr. 1965 Nov 5;90(45):2008-13 PMID: 5833954
  63. UNUSUAL INHERITANCE OF ABO GROUP IN A FAMILY WITH WEAK B ANTIGENS.
    Vox Sang. 1964 May-Jun;9:268-77 PMID: 14170898
  64. A search for autosomal linkage in a trisomic population: blood group frequencies in Mongols.
    Am J Hum Genet. 1962 Dec;14:317-34 PMID: 13976965
  65. STUDIES OF LEUKOCYTE ALKALINE PHOSPHATASE IN MONGOLISM: A POSSIBLE CHROMOSOME MARKER.
    Blood. 1963 Aug;22:165-77 PMID: 14045301
  66. Lactate dehydrogenase variant from human blood: evidence for molecular subunits.
    Science. 1963 Aug 16;141(3581):642-3 PMID: 14014718
  67. Mnifold chromosome abnormalities in leukaemia.
    Lancet. 1962 May 26;1(7239):1098-100 PMID: 14004414
  68. CHROMOSOME DELETION IN A CASE OF RETINOBLASTOMA.
    Ann Hum Genet. 1963 Nov;27:171-4 PMID: 14081487
  69. [THE CRYING CAT SYNDROME: A FURTHER CASE].
    Ann Genet. 1964;7:13-6 PMID: 14242102
  70. PROBABLE DELETION OF THE SHORT ARM OF CHROMOSOME 18.
    Am J Hum Genet. 1964 Sep;16:364-74 PMID: 14207551
  71. PARTIAL DELETION OF THE SHORT ARMS OF A CHROMOSOME OF THE 4-5 GROUP (DENVER).
    Arch Dis Child. 1965 Feb;40:82-5 PMID: 14259280
  72. Genotypic distribution among human autosomal aneuploids: a theoretical consideration.
    Acta Genet Stat Med. 1963;13:67-76 PMID: 13991052
  73. [Exclusion of certain autosomal localizations of blood and serum group genes].
    Ann Genet. 1966;9(1):9-11 PMID: 5295703
  74. "Cri du chat" syndrome. Partial deletion of the short arm of a chromosome No. 5. Report of a case.
    Maandschr Kindergeneeskd. 1965 Aug;33(8):286-98 PMID: 5848077
  75. [Studies on "branched chain oxoacid aciduria" (maple syrup diseases)].
    Med Klin. 1966 Dec 30;61(52):2063-7 PMID: 4385693
Article Info
Journal
Humangenetik
Abbr.
Humangenetik
ISSN
0018-7348
Published
1967-00-00
Pages
85-103
Language
ger
Region
Germany
NLM ID
7607154
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com