Literature DB >> 4136265

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

J Nielsen, U Friedrich, A B Hreidarsson, E Zeuthen.   

Abstract

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Year:  1974        PMID： 4136265     DOI： 10.1007/bf00279014

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


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  4 in total

1.  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

2.  Localization of heterochromatin in human chromosomes.

Authors:  F E Arrighi; T C Hsu
Journal:  Cytogenetics       Date:  1971

3.  A familial variant of chromosome 9.

Authors:  C G Palmer; J Schroder
Journal:  J Med Genet       Date:  1971-06       Impact factor: 6.318

4.  Banding characteristics of paracentric marker constrictions in human chromosomes.

Authors:  P Aula; E Saksela
Journal:  Hereditas       Date:  1972       Impact factor: 3.271
  4 in total
  23 in total

1.  Three cases of minor chromosomal aberrations discovered by prenatal chromosome determination.

Authors:  J Wahlström
Journal:  Humangenetik       Date:  1975

2.  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

3.  Trisomy 9 associated with an enlarged 9qh segment in a liveborn.

Authors:  M Seabright; N Gregson; S Mould
Journal:  Hum Genet       Date:  1976-12-15       Impact factor: 4.132

4.  Morphologic variability of human chromosomes: polymorphism of constitutive heterochromatin.

Authors:  P K Ghosh; I P Singh
Journal:  Hum Genet       Date:  1976-05-19       Impact factor: 4.132

5.  C-band polymorphisms of chromosome 9: quantification by Ce-bands.

Authors:  K Wahedi; I H Pawlowitzki
Journal:  Hum Genet       Date:  1987-09       Impact factor: 4.132

6.  Chromosome polymorphism and twin zygosity.

Authors:  D L Van Dyke; C G Palmer; W E Nance; P L Yu
Journal:  Am J Hum Genet       Date:  1977-09       Impact factor: 11.025

7.  Autosomal deletions 46,XY,del(12)(p11) and 46,XY-46,XY,del(5)(p13) with no effect on physical or mental development.

Authors:  U Friedrich; J Nielsen
Journal:  Humangenetik       Date:  1974-02-21

8.  Heterochromatic polymorphism in spontaneous abortions.

Authors:  L Hemming; C Burns
Journal:  J Med Genet       Date:  1979-10       Impact factor: 6.318

Review 9.  Pericentric inversions. Problems and significance for clinical genetics.

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

10.  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
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