Literature DB >> 5911833

Congenital anomalies due to transmission of a chromosome translocation.

J E Gray, J A Dartnall, R D Creery, J Croudace.   

Abstract

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Mesh：

Year:  1966        PMID： 5911833      PMCID： PMC1012897          DOI： 10.1136/jmg.3.1.59

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  5 in total

1.  Trisomy 9p resulting from maternal 9/21 translocation.

Authors:  I Sŭbrt; B Blehová; B Pallová
Journal:  Hum Genet       Date:  1976-05-19       Impact factor: 4.132

2.  Cytogenetic studies in a patient with a de novo t(Cq-;Gp+).

Authors:  B F Crandall; R E Carrel; G L Adams; R S Sparkes
Journal:  J Med Genet       Date:  1970-12       Impact factor: 6.318

3.  A translocation t (Bq+: Cq-) in a West Indian family and a report of a second family showing a possible long arm group B translocation.

Authors:  M J Thornburn; E H Smith-Read; J E Peck
Journal:  Arch Dis Child       Date:  1969-02       Impact factor: 3.791

4.  Familial transmission of a chromosomal translocation t(2q+;Cp-).

Authors:  C B Lozzio; A A Kattine
Journal:  J Med Genet       Date:  1969-06       Impact factor: 6.318

5.  A new translocation between chromosomes in the 6-12 and 21-22 groups.

Authors:  P M Lord; M D Casey; B M Laurance
Journal:  J Med Genet       Date:  1967-09       Impact factor: 6.318
  5 in total

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