An Unusual Case of Peters Plus Syndrome with Sexual Ambiguity and Absence of Mutations in the B3GALTL Gene

AuthorOlfa Sialaen
AuthorNeila Belguithen
AuthorFaiza Fakhfakhen
Issued Date2013-08-31en
DOIhttps://doi.org/en
URIhttps://brieflands.com/journals/ijp/articles/1371en
KeywordPeters-Plus Syndromeen
KeywordB3GALTL Proteinen
KeywordHumanen
KeywordFacial Dysmorphism with Multiple Malformationsen
KeywordAmbiguous Genitaliaen
PublisherBrieflandsen
TitleAn Unusual Case of Peters Plus Syndrome with Sexual Ambiguity and Absence of Mutations in the B3GALTL Geneen
TypeCase Reporten

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