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- Q91897856 description "artículu científicu espublizáu n'abril de 2020" @default.
- Q91897856 description "im April 2020 veröffentlichter wissenschaftlicher Artikel" @default.
- Q91897856 description "scientific article published on 13 April 2020" @default.
- Q91897856 description "wetenschappelijk artikel" @default.
- Q91897856 description "наукова стаття, опублікована 13 квітня 2020" @default.
- Q91897856 name "A Novel α-Spectrin Pathogenic Variant in Trans to α-Spectrin LELY Causing Neonatal Jaundice With Hemolytic Anemia From Hereditary Pyropoikilocytosis Coexisting With Gilbert Syndrome" @default.
- Q91897856 name "A Novel α-Spectrin Pathogenic Variant in Trans to α-Spectrin LELY Causing Neonatal Jaundice With Hemolytic Anemia From Hereditary Pyropoikilocytosis Coexisting With Gilbert Syndrome" @default.
- Q91897856 type Item @default.
- Q91897856 label "A Novel α-Spectrin Pathogenic Variant in Trans to α-Spectrin LELY Causing Neonatal Jaundice With Hemolytic Anemia From Hereditary Pyropoikilocytosis Coexisting With Gilbert Syndrome" @default.
- Q91897856 label "A Novel α-Spectrin Pathogenic Variant in Trans to α-Spectrin LELY Causing Neonatal Jaundice With Hemolytic Anemia From Hereditary Pyropoikilocytosis Coexisting With Gilbert Syndrome" @default.
- Q91897856 prefLabel "A Novel α-Spectrin Pathogenic Variant in Trans to α-Spectrin LELY Causing Neonatal Jaundice With Hemolytic Anemia From Hereditary Pyropoikilocytosis Coexisting With Gilbert Syndrome" @default.
- Q91897856 prefLabel "A Novel α-Spectrin Pathogenic Variant in Trans to α-Spectrin LELY Causing Neonatal Jaundice With Hemolytic Anemia From Hereditary Pyropoikilocytosis Coexisting With Gilbert Syndrome" @default.
- Q91897856 P1433 Q91897856-574CC506-B2EF-484A-A0F7-E176A24774C9 @default.
- Q91897856 P1476 Q91897856-1FE3FE3A-1D1A-4B6F-A8BF-F55E799919BF @default.
- Q91897856 P2093 Q91897856-10103BDC-D3A1-4578-A504-E619FC50A158 @default.
- Q91897856 P2093 Q91897856-16EAAB01-37CC-4882-9553-75AD091EF85F @default.
- Q91897856 P2093 Q91897856-50D07CF8-1F86-4DDC-A653-7EEE069FB660 @default.
- Q91897856 P2093 Q91897856-7BA03FD6-8A61-4843-BEB2-C8174A4C8B41 @default.
- Q91897856 P2093 Q91897856-A7BE431C-62D1-40BC-9A20-3A333561BDB1 @default.
- Q91897856 P2093 Q91897856-CD290CE5-DBC0-46EF-82EC-C13481C01B98 @default.
- Q91897856 P2093 Q91897856-E67996C2-0D09-430E-80D3-1B7D3130D8AE @default.
- Q91897856 P2093 Q91897856-FFAE95DA-0733-4BA5-BFD3-97DADD36853E @default.
- Q91897856 P31 Q91897856-303DA878-B05D-4382-B96C-F6E3B0CD4CDD @default.
- Q91897856 P356 Q91897856-E60F6366-403C-4113-9D35-EC2B97F096C9 @default.
- Q91897856 P577 Q91897856-773134A5-69BF-46C2-8292-4799FE22E7E1 @default.
- Q91897856 P698 Q91897856-F3EAF16B-152D-4DC3-9AE0-1E442BFA2596 @default.
- Q91897856 P921 Q91897856-40D69BD0-78E8-40BF-898E-5927EB6CDF0B @default.
- Q91897856 P921 Q91897856-92A8F396-1AC3-426E-9BA0-7D1B05319624 @default.
- Q91897856 P921 Q91897856-DA37598E-00BB-448E-99CA-2EAD447AA52C @default.
- Q91897856 P921 Q91897856-E2BB5EDC-6CB1-466C-9DCA-6C298F6A449B @default.
- Q91897856 P356 MPH.0000000000001796 @default.
- Q91897856 P698 32287101 @default.
- Q91897856 P1433 Q15761808 @default.
- Q91897856 P1476 "A Novel α-Spectrin Pathogenic Variant in Trans to α-Spectrin LELY Causing Neonatal Jaundice With Hemolytic Anemia From Hereditary Pyropoikilocytosis Coexisting With Gilbert Syndrome" @default.
- Q91897856 P2093 "Hiromi Ogura" @default.
- Q91897856 P2093 "Hitoshi Kanno" @default.
- Q91897856 P2093 "Masanori Kouwaki" @default.
- Q91897856 P2093 "Shinji Saitoh" @default.
- Q91897856 P2093 "Takahiro Sugiura" @default.
- Q91897856 P2093 "Takao Togawa" @default.
- Q91897856 P2093 "Tomoko Suzuki" @default.
- Q91897856 P2093 "Toshiyuki Yamamoto" @default.
- Q91897856 P31 Q13442814 @default.
- Q91897856 P356 "10.1097/MPH.0000000000001796" @default.
- Q91897856 P577 "2020-04-13T00:00:00Z" @default.
- Q91897856 P698 "32287101" @default.
- Q91897856 P921 Q1145668 @default.
- Q91897856 P921 Q1755487 @default.
- Q91897856 P921 Q5737872 @default.
- Q91897856 P921 Q752216 @default.