D058489DisordersC12.706.316.064C13.351.875.253.064C16.131.939.316.064C19.391.119.06446, XX Disorders of Sex Developmentprns:hasAuthorListauthor listprns:hasNetworkhas networkprns:hasPublicationVenuepublished inprns:informationResourceReferenceinformation resource referenceprns:maxWeightmaximum weightprns:medlineTAjournal title abbreviationprns:meshDescriptorUIMeSH DescriptorUIprns:meshSemanticGroupNameMeSH semantic group nameprns:meshTreeNumberMeSH tree numberprns:minWeightminimum weightprns:numberOfConnectionsnumber of connectionsprns:predicateNodepredicate nodeprns:publicationDatepublication dateprns:yearyearAcademic ArticleArticleDocumentbibo:pmidPubMed IdentifierInformation Resourcevivo:subjectAreaForsubject area forrdf:predicatepredicaterdf:typetyperdfs:labellabelConcept0.5034750.5034751subject area for24356390Shoar Z, Ganguly T, Anderson CE, De Luca F, Suarez EJournal of pediatric endocrinology & metabolism : JPEMShoar Z, Ganguly T, Anderson CE, De Luca F, Suarez E. Absence of WNT4 gene mutation in a patient with MURCS association. J Pediatr Endocrinol Metab. 2014 May; 27(5-6):555-9.J Pediatr Endocrinol Metab2014-05-01T00:00:002014Absence of WNT4 gene mutation in a patient with MURCS association.