Familial clustering of impaired spermatogenesis: no evidence for a common genetic inheritance pattern | Zendy

Judith Gianotten | Zendy

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Familial clustering of impaired spermatogenesis: no evidence for a common genetic inheritance pattern

Author(s) -

Judith Gianotten

Publication year - 2003

Publication title -

human reproduction

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 2.446

H-Index - 226

eISSN - 1460-2350

pISSN - 0268-1161

DOI - 10.1093/humrep/deh008

Subject(s) - male infertility , proband , odds ratio , medicine , fertility , infertility , spermatogenesis , semen analysis , etiology , physiology , genetics , gynecology , biology , pregnancy , population , mutation , environmental health , gene

The aetiology of impaired spermatogenesis is unknown in the majority of cases. Evidence of a contribution of genetic factors is still scarce. Therefore, the aim of our study was to assess whether male factor subfertility due to impaired spermatogenesis has a familial component and to test different genetic models of inheritance.

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