| Literature DB >> 6885076 |
G Cohen, A Manuel, M Cohen, K Fagan, H Grunstein.
Abstract
A patient with a deletion of the distal portion of the long arm (q21) of chromosome Y is described clinically and cytogenetically. The proband has a normal male habitus but with azoospermia. The proband was investigated because of infertility. Male relatives were also investigated cytogenetically. The deleted Y chromosome was measured and compared with the normal Y of male family members. The results suggest that no Y euchromatin was lost.Entities:
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Year: 1983 PMID: 6885076 DOI: 10.1007/bf00279416
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132