21691975

Source:http://linkedlifedata.com/resource/pubmed/id/21691975

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015780, umls-concept:C0019294, umls-concept:C0020792, umls-concept:C0021270, umls-concept:C0205314, umls-concept:C0596611, umls-concept:C0679622, umls-concept:C1421652, umls-concept:C1521721, umls-concept:C1522384, umls-concept:C1710693
pubmed:dateCreated	2011-6-21
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0121103
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/NR5A1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Steroidogenic Factor 1
pubmed:status	MEDLINE
pubmed:issn	0065-2598
pubmed:author	pubmed-author:PhilibertPascalP, pubmed-author:SinhaSunil KSK, pubmed-author:SultanCharlesC, pubmed-author:TenSvetlanaS
pubmed:issnType	Print
pubmed:volume	707
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	149-50
pubmed:meshHeading	pubmed-meshheading:21691975-46, XY Disorders of Sex Development, pubmed-meshheading:21691975-Child, Preschool, pubmed-meshheading:21691975-Female, pubmed-meshheading:21691975-Hernia, Inguinal, pubmed-meshheading:21691975-Humans, pubmed-meshheading:21691975-Mutation, pubmed-meshheading:21691975-Phenotype, pubmed-meshheading:21691975-Steroidogenic Factor 1
pubmed:year	2011
pubmed:articleTitle	Inguinal hernia in a phenotypic female infant may reveal a 46XY sex reversal, supported by the identification of a novel SF1 gene mutation.
pubmed:affiliation	Division of Pediatric Endocrinology, Department of Paediatric Endocrinology, Maimonides Medical Centre, State University of New York Downstate Children's Hospital & Infant's and Children Hospital of Brooklyn at Maimonides, Brooklyn, NY, USA. sanny45@hotmail.com
pubmed:publicationType	Journal Article, Case Reports