Literature DB >> 5911835

A family showing transmission of a translocation between a 6-12 chromosome and a 21-22 chromosome.

J E Gray, J A Dartnall, B G Macnamara.   

Abstract

Mesh：

Year:  1966        PMID： 5911835      PMCID： PMC1012898          DOI： 10.1136/jmg.3.1.62

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


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  1 in total

1.  Chromosome preparations of leukocytes cultured from human peripheral blood.

Authors:  P S MOORHEAD; P C NOWELL; W J MELLMAN; D M BATTIPS; D A HUNGERFORD
Journal:  Exp Cell Res       Date:  1960-09       Impact factor: 3.905
  1 in total
  3 in total

1.  Familial translocation t(3p-;21q+) associated with both Down's and Sturge-Weber's syndrome in unbalanced state.

Authors:  M Habedank; G Kampe
Journal:  Humangenetik       Date:  1975-09-23

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.  Dissociation of a t(12;21) resulting in a normal cell line in two trisomic 21 sons of a nonmosaic t(12;21) father?

Authors:  R C Juberg; R Stallard; P Mowrey; C L Valido
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132
  3 in total

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