|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
4
|
|
pubmed:dateCreated |
1986-9-17
|
|
pubmed:abstractText |
A partial androgen receptor defect was found in a boy with male pseudohermaphroditism and an 11p13 deletion. We hypothesize that a gene responsible for the function or structure of androgen receptors might be localized in the 11p13 band or in close proximity to it.
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|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Aug
|
|
pubmed:issn |
0148-7299
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
24
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
679-84
|
|
pubmed:dateRevised |
2005-11-17
|
|
pubmed:meshHeading |
pubmed-meshheading:3017106-Chromosome Aberrations,
pubmed-meshheading:3017106-Chromosome Deletion,
pubmed-meshheading:3017106-Chromosome Disorders,
pubmed-meshheading:3017106-Chromosomes, Human, 6-12 and X,
pubmed-meshheading:3017106-Genitalia, Male,
pubmed-meshheading:3017106-Humans,
pubmed-meshheading:3017106-Infant, Newborn,
pubmed-meshheading:3017106-Kidney Neoplasms,
pubmed-meshheading:3017106-Male,
pubmed-meshheading:3017106-Receptors, Androgen,
pubmed-meshheading:3017106-Testosterone,
pubmed-meshheading:3017106-Wilms Tumor
|
|
pubmed:year |
1986
|
|
pubmed:articleTitle |
Male pseudohermaphroditism, partial androgen receptors defect, 11p13 deletion: indication of gene localization.
|
|
pubmed:publicationType |
Journal Article,
Case Reports
|
