Literature DB >> 471543

[Clinical and cytogenetic study of a case of trisomy 1q with familial translocation t (1; 5) (q 42; p 15.3) (author's transl)].

M T Duillo, T de Toni, G Cavaliere, G L Bava, A Arslanian, E Bonioli, M G Vianello.   

Abstract

Mesh：

Year:  1979        PMID： 471543

Source DB:  PubMed          Journal:  Pathologica        ISSN： 0031-2983


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  2 in total

1.  Detection of a de novo duplication of 1q32-qter by fluorescence in situ hybridisation in a boy with multiple malformations: further delineation of the trisomy 1q syndrome.

Authors:  H C Duba; M Erdel; J Löffler; L Bereuther; H Fischer; B Utermann; G Utermann
Journal:  J Med Genet       Date:  1997-04       Impact factor: 6.318

2.  An azoospermic male with reciprocal translocation t(1;15) (q11;p11).

Authors:  C López-Ginés; R Gil; M Gregori-Romero; A Pellin
Journal:  Hum Genet       Date:  1987-11       Impact factor: 4.132
  2 in total

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