Literature DB >> 5313145

Familial transmission of an unusual variant of a group C chromosome.

E Tuckerman, J E Gray, J Salmon.   

Abstract

Mesh：

Year:  1970        PMID： 5313145

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


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  5 in total

1.  The constitutional fragility of chromosome 12 in a case of 46,XX,var(12)(gh',RHG,CAG,CBG).

Authors:  E Donti; G Venti; V Bocchini; G Rosi; R Armellini; N Trabalza
Journal:  Hum Genet       Date:  1979-04-17       Impact factor: 4.132

2.  [Partial tetrasomy of number 9 chromosome, and mosaicism in a child with multiple malformations (author's transl)].

Authors:  D Ghymers; B Hermann; C Distèche; J Frederic
Journal:  Humangenetik       Date:  1973-12-10

3.  Presumed trisomy for the short arm of chromosome No. 9 not due to inherited translocation.

Authors:  H Hoehn; W Engel; H Reinwein
Journal:  Humangenetik       Date:  1971

4.  Constitutional chromosomal breakage.

Authors:  F Giraud; S Ayme; J F Mattei; M G Mattei
Journal:  Hum Genet       Date:  1976-10-28       Impact factor: 4.132

5.  Origin of symmetrical triradial chromosomes in human cells.

Authors:  E M Kuhn; E Therman
Journal:  Chromosoma       Date:  1982       Impact factor: 4.316
  5 in total

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