The role of Y chromosome deletions in male infertility.


Autoria(s): Ma, K.; Mallidis, Con; Bhasin, S.
Data(s)

01/05/2000

Resumo

Male infertility affects approximately 2-7% of couples around the world. Over one in ten men who seek help at infertility clinics are diagnosed as severely oligospermic or azoospermic. Recent extensive molecular studies have revealed that deletions in the azoospermia factor region of the long arm of the Y chromosome are associated with severe spermatogenic impairment (absent or severely reduced germ cell development). Genetic research into male infertility, in the last 7 years, has resulted in the isolation of a great number of genes or gene families on the Y chromosome, some of which are believed to influence spermatogenesis.

Identificador

http://pure.qub.ac.uk/portal/en/publications/the-role-of-y-chromosome-deletions-in-male-infertility(47a586d3-25fb-4467-bd9d-0f576b8bd90c).html

http://www.scopus.com/inward/record.url?scp=0034038610&partnerID=8YFLogxK

Idioma(s)

eng

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

Ma , K , Mallidis , C & Bhasin , S 2000 , ' The role of Y chromosome deletions in male infertility. ' European journal of endocrinology / European Federation of Endocrine Societies , vol 142(5) , no. 5 , pp. 418-430 .

Palavras-Chave #/dk/atira/pure/subjectarea/asjc/1300/1310 #Endocrinology
Tipo

article