Matches in Wikidata for { <http://www.wikidata.org/entity/Q89249708> ?p ?o ?g. }
Showing items 1 to 38 of
38
with 100 items per page.
- Q89249708 description "article scientifique publié en 2016" @default.
- Q89249708 description "artículu científicu espublizáu n'abril de 2016" @default.
- Q89249708 description "scientific article published on 19 April 2016" @default.
- Q89249708 description "wetenschappelijk artikel" @default.
- Q89249708 description "наукова стаття, опублікована у квітні 2016" @default.
- Q89249708 name "A rare MeCP2_e1 mutation first described in a male patient with severe neonatal encephalopathy" @default.
- Q89249708 name "A rare MeCP2_e1 mutation first described in a male patient with severe neonatal encephalopathy" @default.
- Q89249708 type Item @default.
- Q89249708 label "A rare MeCP2_e1 mutation first described in a male patient with severe neonatal encephalopathy" @default.
- Q89249708 label "A rare MeCP2_e1 mutation first described in a male patient with severe neonatal encephalopathy" @default.
- Q89249708 prefLabel "A rare MeCP2_e1 mutation first described in a male patient with severe neonatal encephalopathy" @default.
- Q89249708 prefLabel "A rare MeCP2_e1 mutation first described in a male patient with severe neonatal encephalopathy" @default.
- Q89249708 P1433 Q89249708-5488D893-4401-4042-8F51-4D09A4846FFB @default.
- Q89249708 P1476 Q89249708-984B1EF2-290E-4526-A3CF-FDADAADE11B8 @default.
- Q89249708 P2093 Q89249708-45E8A3BF-1D75-4C65-B98D-1F8C404E29CB @default.
- Q89249708 P2093 Q89249708-621E9214-CF1D-4C5A-8B30-1F1F8F3E3EE4 @default.
- Q89249708 P304 Q89249708-877B23C6-438A-45A0-B965-F36DA2DD74C5 @default.
- Q89249708 P31 Q89249708-8664CE23-E6AB-47F4-B0BE-C95C1FC93CC0 @default.
- Q89249708 P356 Q89249708-1F4D9F93-2166-4C14-A218-B5EF9A138776 @default.
- Q89249708 P433 Q89249708-9149C61C-5085-46C0-922E-BD40955F5F60 @default.
- Q89249708 P478 Q89249708-E657310F-B256-403E-AEAF-A53ECB8A29FC @default.
- Q89249708 P577 Q89249708-A38316A2-1618-4703-A315-981B80B4A967 @default.
- Q89249708 P698 Q89249708-B2140229-20F5-42EB-8FF8-362C2B30094E @default.
- Q89249708 P921 Q89249708-672CC91F-FC7A-49EF-9DD5-DC5DB2EA3AD2 @default.
- Q89249708 P356 AJMG.A.37665 @default.
- Q89249708 P698 27090848 @default.
- Q89249708 P1433 Q4744254 @default.
- Q89249708 P1476 "A rare MeCP2_e1 mutation first described in a male patient with severe neonatal encephalopathy" @default.
- Q89249708 P2093 "Omri David Soffer" @default.
- Q89249708 P2093 "Richard Sidlow" @default.
- Q89249708 P304 "1881-1883" @default.
- Q89249708 P31 Q13442814 @default.
- Q89249708 P356 "10.1002/AJMG.A.37665" @default.
- Q89249708 P433 "7" @default.
- Q89249708 P478 "170" @default.
- Q89249708 P577 "2016-04-19T00:00:00Z" @default.
- Q89249708 P698 "27090848" @default.
- Q89249708 P921 Q5832339 @default.