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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
2
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pubmed:dateCreated |
2006-3-31
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pubmed:abstractText |
To investigate the frequency and potential impact of mutations and polymorphisms in the CFTR gene and deletions in AZF locus of the Y chromosome in patients with azoospermia (AZOO), cryptozoospermia (CRYPTO) or oligoasthenoteratozoospermia (OAT) who were to be included in an assisted reproductive technologies (ART) program.
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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:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0024-7758
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
51
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
120-7
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:16572913-Adult,
pubmed-meshheading:16572913-Case-Control Studies,
pubmed-meshheading:16572913-Chromosome Deletion,
pubmed-meshheading:16572913-Chromosomes, Human, Y,
pubmed-meshheading:16572913-Cystic Fibrosis Transmembrane Conductance Regulator,
pubmed-meshheading:16572913-DNA Mutational Analysis,
pubmed-meshheading:16572913-Gene Expression Regulation,
pubmed-meshheading:16572913-Gene Frequency,
pubmed-meshheading:16572913-Genetic Predisposition to Disease,
pubmed-meshheading:16572913-Humans,
pubmed-meshheading:16572913-Infertility, Male,
pubmed-meshheading:16572913-Male,
pubmed-meshheading:16572913-Middle Aged,
pubmed-meshheading:16572913-Oligospermia,
pubmed-meshheading:16572913-Probability,
pubmed-meshheading:16572913-Risk Assessment,
pubmed-meshheading:16572913-Sensitivity and Specificity
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pubmed:year |
2006
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pubmed:articleTitle |
Molecular analysis of defects in the CFTR gene and AZF locus of the Y chromosome in male infertility.
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pubmed:affiliation |
Medical Genetics Department, Institute of Mother and Child, Warsaw, Poland. agnieszk@imid.med.pl
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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