Matches in Wikidata for { <http://www.wikidata.org/entity/Q91324476> ?p ?o ?g. }
Showing items 1 to 46 of
46
with 100 items per page.
- Q91324476 description "artículu científicu espublizáu n'ochobre de 2015" @default.
- Q91324476 description "im Oktober 2015 veröffentlichter wissenschaftlicher Artikel" @default.
- Q91324476 description "scientific article published on 28 October 2015" @default.
- Q91324476 description "wetenschappelijk artikel" @default.
- Q91324476 description "наукова стаття, опублікована в жовтні 2015" @default.
- Q91324476 name "BCAP31 Mutation Causing a Syndrome of Congenital Dystonia, Facial Dysorphism and Central Hypomyelination Discovered Using Exome Sequencing" @default.
- Q91324476 name "BCAP31 Mutation Causing a Syndrome of Congenital Dystonia, Facial Dysorphism and Central Hypomyelination Discovered Using Exome Sequencing" @default.
- Q91324476 type Item @default.
- Q91324476 label "BCAP31 Mutation Causing a Syndrome of Congenital Dystonia, Facial Dysorphism and Central Hypomyelination Discovered Using Exome Sequencing" @default.
- Q91324476 label "BCAP31 Mutation Causing a Syndrome of Congenital Dystonia, Facial Dysorphism and Central Hypomyelination Discovered Using Exome Sequencing" @default.
- Q91324476 prefLabel "BCAP31 Mutation Causing a Syndrome of Congenital Dystonia, Facial Dysorphism and Central Hypomyelination Discovered Using Exome Sequencing" @default.
- Q91324476 prefLabel "BCAP31 Mutation Causing a Syndrome of Congenital Dystonia, Facial Dysorphism and Central Hypomyelination Discovered Using Exome Sequencing" @default.
- Q91324476 P1433 Q91324476-B0F1269D-DADD-4FE9-88B7-CD656C951152 @default.
- Q91324476 P1476 Q91324476-BA0AE6C3-DDA3-44A0-B578-43ADE52B91EB @default.
- Q91324476 P2093 Q91324476-01C8E3EB-F3F6-4FA1-9234-EED775E69CAF @default.
- Q91324476 P2093 Q91324476-21479BEF-34F8-4F5A-9B20-159B48C3A49C @default.
- Q91324476 P2093 Q91324476-A944C05B-51D7-436A-8BE9-E15F56A24296 @default.
- Q91324476 P2093 Q91324476-D9E3EE12-8EE8-4772-A2B5-DE8D53FBF19C @default.
- Q91324476 P2093 Q91324476-FE53BE08-388B-4906-AAF6-D7B059442ECA @default.
- Q91324476 P304 Q91324476-8AFA3075-48EE-4B58-9880-DE250EF324B1 @default.
- Q91324476 P31 Q91324476-13a89119-e2d6-4f41-af5f-f65e6e458cc2 @default.
- Q91324476 P31 Q91324476-7CB58242-6299-4D69-88D9-53B5CBD08C56 @default.
- Q91324476 P356 Q91324476-0DB4EA57-4B6F-42E9-9F96-CDC2BD8FED48 @default.
- Q91324476 P433 Q91324476-D0DA1324-9F40-4BB6-A474-106F255F1240 @default.
- Q91324476 P478 Q91324476-30C9F0A1-5D13-4FF3-8CB0-FABA0FC1AB12 @default.
- Q91324476 P577 Q91324476-CADC7862-EDD9-40CC-ADBE-C2B23D36AFE2 @default.
- Q91324476 P698 Q91324476-0BF1FE8F-BB8F-4ECF-B746-E8784B5FA119 @default.
- Q91324476 P932 Q91324476-7873DA67-5E85-45B4-A534-747DE9A1C7EF @default.
- Q91324476 P356 MDC3.12250 @default.
- Q91324476 P698 30713915 @default.
- Q91324476 P1433 Q27725493 @default.
- Q91324476 P1476 "BCAP31 Mutation Causing a Syndrome of Congenital Dystonia, Facial Dysorphism and Central Hypomyelination Discovered Using Exome Sequencing" @default.
- Q91324476 P2093 "Deborah A Hall" @default.
- Q91324476 P2093 "Elizabeth Berry-Kravis" @default.
- Q91324476 P2093 "Padmaja Vittal" @default.
- Q91324476 P2093 "Rong Mao" @default.
- Q91324476 P2093 "Shale Dames" @default.
- Q91324476 P304 "197-199" @default.
- Q91324476 P31 Q13442814 @default.
- Q91324476 P31 Q2782326 @default.
- Q91324476 P356 "10.1002/MDC3.12250" @default.
- Q91324476 P433 "2" @default.
- Q91324476 P478 "3" @default.
- Q91324476 P577 "2015-10-28T00:00:00Z" @default.
- Q91324476 P698 "30713915" @default.
- Q91324476 P932 "6353445" @default.