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Article

Inguinal hernia in a phenotypic female infant may reveal a 46XY sex reversal, supported by the identification of a novel SF1 gene mutation.

Advances in experimental medicine and biology - 1 Jan 2011

Sinha Sunil K, Philibert Pascal, Sultan Charles, Ten Svetlana

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Share to Child, Preschool
Share to Disorder of Sex Development, 46,XY
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Steroidogenic Factor 1

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PMID: 21691975
DOI: 10.1007/978-1-4419-8002-1_33

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Inguinal hernia in a phenotypic female infant may reveal a 46XY sex reversal, supported by the identification of a novel SF1 gene mutation.PMID 21691975Read ↗

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