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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6
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pubmed:dateCreated |
2000-12-21
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pubmed:abstractText |
Although the frequent association between distal 10q monosomy and urogenital anomalies suggests the presence of a gene(s) for urogenital development on distal 10q, molecular deletion mapping has not been performed for the putative gene(s). In this study, we examined genotype-phenotype correlations in patients with distal 10q monosomy.
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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 |
Dec
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pubmed:issn |
0085-2538
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pubmed:author |
|
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pubmed:issnType |
Print
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pubmed:volume |
58
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2281-90
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11115062-Adolescent,
pubmed-meshheading:11115062-Child,
pubmed-meshheading:11115062-Child, Preschool,
pubmed-meshheading:11115062-Chromosome Aberrations,
pubmed-meshheading:11115062-Chromosome Mapping,
pubmed-meshheading:11115062-Chromosomes, Human, Pair 10,
pubmed-meshheading:11115062-Cryptorchidism,
pubmed-meshheading:11115062-Female,
pubmed-meshheading:11115062-Gene Deletion,
pubmed-meshheading:11115062-Humans,
pubmed-meshheading:11115062-Hypospadias,
pubmed-meshheading:11115062-In Situ Hybridization, Fluorescence,
pubmed-meshheading:11115062-Infant,
pubmed-meshheading:11115062-Kidney,
pubmed-meshheading:11115062-Kidney Diseases, Cystic,
pubmed-meshheading:11115062-Male,
pubmed-meshheading:11115062-Microsatellite Repeats,
pubmed-meshheading:11115062-Penis,
pubmed-meshheading:11115062-Vesico-Ureteral Reflux,
pubmed-meshheading:11115062-Vulva
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pubmed:year |
2000
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pubmed:articleTitle |
Genetic evidence for a novel gene(s) involved in urogenital development on 10q26.
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pubmed:affiliation |
Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan. t-ogata@po.iijnet.or.jp
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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