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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2-3
|
pubmed:dateCreated |
1987-8-28
|
pubmed:abstractText |
The second child of a non consanguineous couple had a male phenotype with two intrascrotal testes of normal size however a scrotum bifidum was noted. The karyotype of the child was 46 XX and the parents one's was normal. No Y specific sequence was detected by using four Y specific probes (47 B, 12 F3, 52 D and 118). During the first semester of life, hormonal investigations showed a normal testicular function.
|
pubmed:language |
fre
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
May
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pubmed:issn |
0021-7743
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
35
|
pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
165-72
|
pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:3612094-Androgens,
pubmed-meshheading:3612094-Humans,
pubmed-meshheading:3612094-Infant, Newborn,
pubmed-meshheading:3612094-Male,
pubmed-meshheading:3612094-Phenotype,
pubmed-meshheading:3612094-Sex Determination Analysis,
pubmed-meshheading:3612094-Sex Differentiation,
pubmed-meshheading:3612094-Testis,
pubmed-meshheading:3612094-X Chromosome
|
pubmed:year |
1987
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pubmed:articleTitle |
[An XX male newborn infant. A genetic and endocrinologic study].
|
pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|