D011218DisordersC10.597.606.643.690C16.131.077.730C16.131.260.700C16.320.180.700C18.654.726.500.740Prader-Willi Syndromeprns: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:labellabelConcept0.3751730.18971619subject area for17036336Bittel DC, Kibiryeva N, McNulty SG, Driscoll DJ, Butler MG, White RAAmerican journal of medical genetics. Part ABittel DC, Kibiryeva N, McNulty SG, Driscoll DJ, Butler MG, White RA. Whole genome microarray analysis of gene expression in an imprinting center deletion mouse model of Prader-Willi syndrome. Am J Med Genet A. 2007 Mar 01; 143A(5):422-9.Am J Med Genet A2007-03-01T00:00:002007Whole genome microarray analysis of gene expression in an imprinting center deletion mouse model of Prader-Willi syndrome.17036338Butler MG, Theodoro MF, Bittel DC, Kuipers PJ, Driscoll DJ, Talebizadeh ZAmerican journal of medical genetics. Part AButler MG, Theodoro MF, Bittel DC, Kuipers PJ, Driscoll DJ, Talebizadeh Z. X-chromosome inactivation patterns in females with Prader-Willi syndrome. Am J Med Genet A. 2007 Mar 01; 143A(5):469-75.Am J Med Genet A2007-03-01T00:00:002007X-chromosome inactivation patterns in females with Prader-Willi syndrome.17236194Bittel DC, Kibiryeva N, Sell SM, Strong TV, Butler MGAmerican journal of medical genetics. Part ABittel DC, Kibiryeva N, Sell SM, Strong TV, Butler MG. Whole genome microarray analysis of gene expression in Prader-Willi syndrome. Am J Med Genet A. 2007 Mar 01; 143A(5):430-42.Am J Med Genet A2007-03-01T00:00:002007Whole genome microarray analysis of gene expression in Prader-Willi syndrome.18266248Butler MG, Fischer W, Kibiryeva N, Bittel DCAmerican journal of medical genetics. Part AButler MG, Fischer W, Kibiryeva N, Bittel DC. Array comparative genomic hybridization (aCGH) analysis in Prader-Willi syndrome. Am J Med Genet A. 2008 Apr 01; 146A(7):854-60.Am J Med Genet A2008-04-01T00:00:002008Array comparative genomic hybridization (aCGH) analysis in Prader-Willi syndrome.20082457Butler MG, Bittel DC, Kibiryeva N, Cooley LD, Yu SAmerican journal of medical genetics. Part AButler MG, Bittel DC, Kibiryeva N, Cooley LD, Yu S. An interstitial 15q11-q14 deletion: expanded Prader-Willi syndrome phenotype. Am J Med Genet A. 2010 Feb; 152A(2):404-8.Am J Med Genet A2010-02-01T00:00:002010An interstitial 15q11-q14 deletion: expanded Prader-Willi syndrome phenotype.