Literature DB >> 4140842

Marker chromosomes in parents of spontaneous abortuses.

S Holbek, U Friedrich, J G Lauritsen, J Therkelsen.   

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Year:  1974        PMID: 4140842     DOI: 10.1007/bf00281007

Source DB:  PubMed          Journal:  Humangenetik        ISSN: 0018-7348


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  13 in total

1.  [FAMILIAL AND ANEUPLOID MARKER CHROMOSOMES. POSSIBLE ROLE OF CHROMOSOME INTERACTION].

Authors:  J DE GROUCHY; S THIEFFRY; M ARTHUIS; J GERBEAUX; S POUPINET; C SALMON; M LAMY
Journal:  Ann Genet       Date:  1964

2.  ENLARGED SHORT ARM OF A SMALL ACROCENTRIC CHROMOSOME IN GRANDFATHER, MOTHER AND CHILD, THE LATTER WITH DOWN'S SYNDROME.

Authors:  A J THERKELSEN
Journal:  Cytogenetics       Date:  1964

3.  CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). I. DATA ON A CONSECUTIVE SERIES OF PATIENTS REFERRED FOR GENETIC COUNSELLING AND DIAGNOSIS.

Authors:  J L HAMERTON; F GIANNELLI; P E POLANI
Journal:  Cytogenetics       Date:  1965

4.  Frequency of 9qh+ and risk of chromosome aberrations in the progeny of individuals with 9qh+.

Authors:  J Nielsen; U Friedrich; A B Hreidarsson; E Zeuthen
Journal:  Humangenetik       Date:  1974

5.  New staining methods for chromosomes.

Authors:  H A Lubs; W H McKenzie; S R Patil; S Merrick
Journal:  Methods Cell Biol       Date:  1973       Impact factor: 1.441

6.  Location of satellite and homogeneous DNA sequences on human chromosomes.

Authors:  K W Jones; G Corneo
Journal:  Nat New Biol       Date:  1971-10-27

7.  Short arm enlargement in acrocentric chromosomes.

Authors:  V E Sands
Journal:  Am J Hum Genet       Date:  1969-05       Impact factor: 11.025

8.  The chromosomal location of human satellite DNA 3.

Authors:  K W Jones; J Prosser; G Corneo; E Ginelli
Journal:  Chromosoma       Date:  1973-07-18       Impact factor: 4.316

9.  Human karyotype polymorphism. I. Routine and fluorescence microscopic investigation of chromosomes in a normal adult population.

Authors:  A V Mikelsaar; S J Tüür; M E Käosaar
Journal:  Humangenetik       Date:  1973

10.  Length of the Y chromosome in criminal males.

Authors:  J Nielsen; U Friedrich
Journal:  Clin Genet       Date:  1972       Impact factor: 4.438

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  7 in total

1.  Association of pericentric inversion of chromosome 9 and reproductive failure in ten unrelated families.

Authors:  J Boué; J L Taillemite; P Hazael-Massieux; C Léonard; A Boué
Journal:  Humangenetik       Date:  1975-09-20

2.  A rare chromosome 5 heterochromatic variant derived from insertion of 9qh satellite 3 sequences.

Authors:  L Doneda; P Gandolfi; G Nocera; L Larizza
Journal:  Chromosome Res       Date:  1998-08       Impact factor: 5.239

3.  Cytogenetic survey in couples with recurrent fetal wastage.

Authors:  J P Fryns; A Kleczkowska; E Kubień; P Petit; H Van den Berghe
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

Review 4.  Aspects of evaluation, significance, and evolution of human C-band heteromorphism.

Authors:  B Erdtmann
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

Review 5.  Pericentric inversions. Problems and significance for clinical genetics.

Authors:  P Kaiser
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

6.  C heterochromatin variation in couples with recurrent early abortions.

Authors:  A Maes; C Staessen; L Hens; E Vamos; M Kirsch-Volders; M C Lauwers; E Defrise-Gussenhoven; C Susanne
Journal:  J Med Genet       Date:  1983-10       Impact factor: 6.318

7.  Intercalar satellites of human acrocentric chromosomes as a cytological manifestation of polymorphism in GC-rich material?

Authors:  P Balícek; J Zizka
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

  7 in total

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