Literature DB >> 4254302

The chromosomal constitution of 165 human translocations involving D group chromosomes identified by autoradiography.

M M Cohen.   

Abstract

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Year:  1971        PMID: 4254302

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


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  19 in total

1.  Klinefelter's syndrome associated with a D/D translocation.

Authors:  M Sparagana; G P Smith
Journal:  J Med Genet       Date:  1975-09       Impact factor: 6.318

2.  Transmission of a t(13q22q) chromosome observed in three generations with segregation of the translocation D1-trisomy syndrome.

Authors:  T Abe; M Morita; K Kawai; S Misawa; H Kanai; G Hirose; H Fujita
Journal:  Humangenetik       Date:  1975-09-20

3.  Delineation of Robertsonian translocations in man by means of chromosome banding.

Authors:  F S Hill; R L Summitt
Journal:  Eur J Pediatr       Date:  1977-11-04       Impact factor: 3.183

4.  Structure and inheritance of some heterozygous Robertsonian translocation in man.

Authors:  A Daniel; P R Lam-Po-Tang
Journal:  J Med Genet       Date:  1976-10       Impact factor: 6.318

5.  Four familial translocations ascertained through spontaneous abortions.

Authors:  D H Carr; M M Gedeon
Journal:  Hum Genet       Date:  1976-01-28       Impact factor: 4.132

6.  Association of D/D translocations with fetal wastage and aneuploidy. A report of four families.

Authors:  P M Fernhoff; D N Singh; J Hanson; S Trusler; C R Dumont; A T Chen
Journal:  J Med Genet       Date:  1976-10       Impact factor: 6.318

7.  Homologous Robertsonian translocation (21q21q) and abortions.

Authors:  T Sudha; P M Gopinath
Journal:  Hum Genet       Date:  1990-07       Impact factor: 4.132

8.  Analysis of meiotic segregation in a man heterozygous for a 13;15 Robertsonian translocation and a review of the literature.

Authors:  F Pellestor
Journal:  Hum Genet       Date:  1990-06       Impact factor: 4.132

9.  Familial translocation 15-22. A possible cause for abortions in female carriers.

Authors:  K Fried; J Bukovsky; M Rosenblatt; G Mundel
Journal:  J Med Genet       Date:  1974-09       Impact factor: 6.318

10.  A girl with the Prader-Willi syndrome and Robertsonian translocation 45,XX,t(14;15)(p11;q11) which was present in three normal family members.

Authors:  A Smith; M Noel
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

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