Literature DB >> 316666

Clinical significance of the satellited short arm of human chromosome 17 (17ps +) : a rare heteromorphism?

R S Verma, S Ved Brat, J Warman, H Dosik.   

Abstract

A 43-year-old impotent male Caucasian had a chromosomal constitution of 46,XY,17ps+. The satellited chromosome 17 was also present in his sister. There is no suggestive evidence that this satellited chromosome causes any clinical abnormality. Based on multiple banding techniques, it is concluded that the 17ps+ is a rare chromosomal heteromorphism.

Entities:  

Mesh:

Year:  1979        PMID: 316666

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


  1 in total

1.  Chromosome 17 has a real fragile site at p12.

Authors:  F Shabtai; D Klar; I Halbrecht
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.