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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
2007-4-11
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pubmed:abstractText |
Cryptorchidism is one of the most common congenital anomalies and is associated with increased risk for infertility and testicular cancer later in life. Findings from animal models and small clinical studies suggest that the posterior HOX genes (paralogs 9-13) could be potential candidate genes for cryptorchidism and that the HOX genes are functionally redundant within paralogous groups.
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pubmed:grant |
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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 |
Apr
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|
pubmed:issn |
1542-0752
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
79
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
269-75
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:17216618-Alleles,
pubmed-meshheading:17216618-Alternative Splicing,
pubmed-meshheading:17216618-Case-Control Studies,
pubmed-meshheading:17216618-Cryptorchidism,
pubmed-meshheading:17216618-Gene Frequency,
pubmed-meshheading:17216618-Genetic Variation,
pubmed-meshheading:17216618-Haplotypes,
pubmed-meshheading:17216618-Homeodomain Proteins,
pubmed-meshheading:17216618-Humans,
pubmed-meshheading:17216618-Infant,
pubmed-meshheading:17216618-Infant, Newborn,
pubmed-meshheading:17216618-Male,
pubmed-meshheading:17216618-Regulatory Elements, Transcriptional
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pubmed:year |
2007
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pubmed:articleTitle |
Allelic variants in HOX genes in cryptorchidism.
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pubmed:affiliation |
Division of Human Genetics and Molecular Biology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA. wangy@email.chop.edu
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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