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

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作者信息

López-Ginés C, Gil R, Gregori-Romero M, Pellin A

机构信息

Department of Pathology, Faculty of Medicine, University of Valencia, Spain.

出版信息

Hum Genet. 1987 Nov;77(3):294. doi: 10.1007/BF00284491.

DOI:10.1007/BF00284491

PMID:3679215

Abstract

The authors report on a case of 1;15 translocation and request contact with any colleagues who have observed similar cases.

摘要

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Hum Genet. 1987 Nov;77(3):294. doi: 10.1007/BF00284491.

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本文引用的文献

The ascertainment and implications of an unbalanced translocation in the neonate. Familial 1:15 translocation.

Aust Paediatr J. 1980 Sep;16(3):196-200. doi: 10.1111/j.1440-1754.1980.tb01296.x.

A girl with 46,XX,t(1;15) karyotype. Cytogenetic and clinical observations.

Clin Genet. 1975 Sep;8(3):213-7. doi: 10.1111/j.1399-0004.1975.tb01496.x.

A (1;15) translocation, balanced, 46 chromosomes. Repository identification No. GM-126.

Cytogenet Cell Genet. 1975;14(1):84-6. doi: 10.1159/000130324.

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

Pathologica. 1979 Mar-Apr;71(1012):223-34.

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