D013255Chemicals & DrugsD08.244.453.493.500D08.244.453.915.760D08.811.682.690.708.170.463.500D08.811.682.690.708.170.915.760D12.776.422.220.453.493.500D12.776.422.220.453.915.760Steroid 21-Hydroxylaseprns: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:labellabelConcept23284009Merke DP, Chen W, Morissette R, Xu Z, Van Ryzin C, Sachdev V, Hannoush H, Shanbhag SM, Acevedo AT, Nishitani M, Arai AE, McDonnell NBThe Journal of clinical endocrinology and metabolismTenascin-X haploinsufficiency associated with Ehlers-Danlos syndrome in patients with congenital adrenal hyperplasia. J Clin Endocrinol Metab. 2013 Feb; 98(2):E379-87.J Clin Endocrinol Metab2013-01-02T00:00:002013Tenascin-X haploinsufficiency associated with Ehlers-Danlos syndrome in patients with congenital adrenal hyperplasia.22886582Chen W, Xu Z, Nishitani M, Van Ryzin C, McDonnell NB, Merke DPHuman geneticsComplement component 4 copy number variation and CYP21A2 genotype associations in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Hum Genet. 2012 Dec; 131(12):1889-94.Hum Genet2012-08-12T00:00:002012Complement component 4 copy number variation and CYP21A2 genotype associations in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.0.459030.446742subject area for