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- Q91979853 description "article scientifique publié en 2020" @default.
- Q91979853 description "artículu científicu espublizáu n'abril de 2020" @default.
- Q91979853 description "scientific article published on 15 April 2020" @default.
- Q91979853 description "wetenschappelijk artikel" @default.
- Q91979853 description "наукова стаття, опублікована 15 квітня 2020" @default.
- Q91979853 description "գիտական հոդված հրատարակված 2020 թվականի ապրիլի 15-ին" @default.
- Q91979853 name "Recognizing the unique prenatal phenotype of Prader-Willi Syndrome (PWS) indicates the need for a diagnostic methylation test" @default.
- Q91979853 name "Recognizing the unique prenatal phenotype of Prader-Willi Syndrome (PWS) indicates the need for a diagnostic methylation test" @default.
- Q91979853 type Item @default.
- Q91979853 label "Recognizing the unique prenatal phenotype of Prader-Willi Syndrome (PWS) indicates the need for a diagnostic methylation test" @default.
- Q91979853 label "Recognizing the unique prenatal phenotype of Prader-Willi Syndrome (PWS) indicates the need for a diagnostic methylation test" @default.
- Q91979853 prefLabel "Recognizing the unique prenatal phenotype of Prader-Willi Syndrome (PWS) indicates the need for a diagnostic methylation test" @default.
- Q91979853 prefLabel "Recognizing the unique prenatal phenotype of Prader-Willi Syndrome (PWS) indicates the need for a diagnostic methylation test" @default.
- Q91979853 P1433 Q91979853-B02557CB-EAB1-47F7-AEEB-1EB32C01BECB @default.
- Q91979853 P1476 Q91979853-75C4E19D-8CBD-4906-B186-E6957146055E @default.
- Q91979853 P2093 Q91979853-1BB7AA4E-D36D-4987-858E-F8B1FF71F105 @default.
- Q91979853 P2093 Q91979853-44588822-132D-4537-AC6C-9ADB28478875 @default.
- Q91979853 P2093 Q91979853-82D8434D-5B5F-4111-9F1A-9B3D80F3243D @default.
- Q91979853 P2093 Q91979853-C0512D02-1B94-469F-8516-E489B1D65784 @default.
- Q91979853 P2093 Q91979853-E50E98C4-5FA7-469F-B4BE-24EA5D54F3A9 @default.
- Q91979853 P31 Q91979853-16308DA2-2AE3-4D97-9CF7-1C05BC491418 @default.
- Q91979853 P356 Q91979853-844C074B-9304-4F14-8755-75D67A0B0C91 @default.
- Q91979853 P50 Q91979853-2EAE0E67-A232-4CDA-815E-DF594D2FAF76 @default.
- Q91979853 P50 Q91979853-3179A89A-8ED7-4118-9DF4-399D164D08AD @default.
- Q91979853 P577 Q91979853-253B6C69-6119-4615-B7FF-B80AD331C74C @default.
- Q91979853 P698 Q91979853-CA3C41A5-2F16-4253-A182-FFBE564641CC @default.
- Q91979853 P921 Q91979853-B1830E93-DAAA-42CB-A624-FE1111A7CC62 @default.
- Q91979853 P356 PD.5712 @default.
- Q91979853 P698 32297338 @default.
- Q91979853 P1433 Q15760059 @default.
- Q91979853 P1476 "Recognizing the unique prenatal phenotype of Prader-Willi Syndrome (PWS) indicates the need for a diagnostic methylation test" @default.
- Q91979853 P2093 "Abdalla Salama" @default.
- Q91979853 P2093 "Harry J Hirsch" @default.
- Q91979853 P2093 "Hen Y Sela" @default.
- Q91979853 P2093 "Noa Gross Even Zohar" @default.
- Q91979853 P2093 "Varda Gross-Tsur" @default.
- Q91979853 P31 Q13442814 @default.
- Q91979853 P356 "10.1002/PD.5712" @default.
- Q91979853 P50 Q110771660 @default.
- Q91979853 P50 Q90875724 @default.
- Q91979853 P577 "2020-04-15T00:00:00Z" @default.
- Q91979853 P698 "32297338" @default.
- Q91979853 P921 Q594013 @default.