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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
1
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pubmed:dateCreated |
2003-12-22
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pubmed:abstractText |
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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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0268-1161
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
19
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
71-6
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:14688159-Adult,
pubmed-meshheading:14688159-Case-Control Studies,
pubmed-meshheading:14688159-Cluster Analysis,
pubmed-meshheading:14688159-Female,
pubmed-meshheading:14688159-Genes, Dominant,
pubmed-meshheading:14688159-Genes, Recessive,
pubmed-meshheading:14688159-Humans,
pubmed-meshheading:14688159-Infertility, Female,
pubmed-meshheading:14688159-Infertility, Male,
pubmed-meshheading:14688159-Inheritance Patterns,
pubmed-meshheading:14688159-Male,
pubmed-meshheading:14688159-Models, Genetic,
pubmed-meshheading:14688159-Prevalence,
pubmed-meshheading:14688159-Semen,
pubmed-meshheading:14688159-Spermatogenesis
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pubmed:year |
2004
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pubmed:articleTitle |
Familial clustering of impaired spermatogenesis: no evidence for a common genetic inheritance pattern.
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pubmed:affiliation |
Center for Reproductive Medicine, Academic Medical Center, Amsterdam, The Netherlands. J.Gianotten@amc.uva.nl
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pubmed:publicationType |
Journal Article
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