Matches in Wikidata for { <http://www.wikidata.org/entity/Q71861823> ?p ?o ?g. }
Showing items 1 to 42 of
42
with 100 items per page.
- Q71861823 description "artikull shkencor i botuar më 01 janar 1996" @default.
- Q71861823 description "artículu científicu espublizáu en xineru de 1996" @default.
- Q71861823 description "im Jahr 1996 veröffentlichter wissenschaftlicher Artikel" @default.
- Q71861823 description "scientific article published on 01 January 1996" @default.
- Q71861823 description "wetenschappelijk artikel" @default.
- Q71861823 description "наукова стаття, опублікована в січні 1996" @default.
- Q71861823 name "Crouzon syndrome: previously unrecognized deletion, duplication, and point mutation within FGFR2 gene" @default.
- Q71861823 name "Crouzon syndrome: previously unrecognized deletion, duplication, and point mutation within FGFR2 gene" @default.
- Q71861823 name "Crouzon syndrome: previously unrecognized deletion, duplication, and point mutation within FGFR2 gene" @default.
- Q71861823 type Item @default.
- Q71861823 label "Crouzon syndrome: previously unrecognized deletion, duplication, and point mutation within FGFR2 gene" @default.
- Q71861823 label "Crouzon syndrome: previously unrecognized deletion, duplication, and point mutation within FGFR2 gene" @default.
- Q71861823 label "Crouzon syndrome: previously unrecognized deletion, duplication, and point mutation within FGFR2 gene" @default.
- Q71861823 prefLabel "Crouzon syndrome: previously unrecognized deletion, duplication, and point mutation within FGFR2 gene" @default.
- Q71861823 prefLabel "Crouzon syndrome: previously unrecognized deletion, duplication, and point mutation within FGFR2 gene" @default.
- Q71861823 prefLabel "Crouzon syndrome: previously unrecognized deletion, duplication, and point mutation within FGFR2 gene" @default.
- Q71861823 P1433 Q71861823-B9E22FAB-167D-4B05-B81D-4C1479C9A817 @default.
- Q71861823 P1476 Q71861823-47A986C0-F454-4A0B-B33D-E1F702364FE8 @default.
- Q71861823 P2093 Q71861823-5D5DBF5F-5AA7-4F74-9CE5-33393728BF9D @default.
- Q71861823 P2093 Q71861823-78E01160-FFF6-4EB1-9BE3-A12A5788A961 @default.
- Q71861823 P2093 Q71861823-E028895C-2507-40C8-A8FF-C82A7729B37B @default.
- Q71861823 P304 Q71861823-80BA9B63-9F75-46F1-92DF-4ED8C4F36668 @default.
- Q71861823 P31 Q71861823-D6441A7C-3170-4EF1-9E89-0FEAC4434DE8 @default.
- Q71861823 P356 Q71861823-D122D4E6-3716-458A-AA8A-179A8447C902 @default.
- Q71861823 P433 Q71861823-F13AB276-DC5D-4506-A5F0-2BA199F3C7E9 @default.
- Q71861823 P478 Q71861823-DA58BE69-78B4-4863-9840-BF6ACC5B2F7C @default.
- Q71861823 P577 Q71861823-A70A3D4F-26AA-4D9C-AF97-5CE0FD6C2FDA @default.
- Q71861823 P698 Q71861823-E1571597-1D7F-4F41-BE40-FAD12C75D324 @default.
- Q71861823 P356 (SICI)1098-1004(1996)8:4%3C386::AID-HUMU18%3E3.0.CO;2-Z @default.
- Q71861823 P698 8956050 @default.
- Q71861823 P1433 Q5937269 @default.
- Q71861823 P1476 "Crouzon syndrome: previously unrecognized deletion, duplication, and point mutation within FGFR2 gene" @default.
- Q71861823 P2093 "D Steinberger" @default.
- Q71861823 P2093 "J B Mulliken" @default.
- Q71861823 P2093 "U Müller" @default.
- Q71861823 P304 "386-390" @default.
- Q71861823 P31 Q13442814 @default.
- Q71861823 P356 "10.1002/(SICI)1098-1004(1996)8:4<386::AID-HUMU18>3.0.CO;2-Z" @default.
- Q71861823 P433 "4" @default.
- Q71861823 P478 "8" @default.
- Q71861823 P577 "1996-01-01T00:00:00Z" @default.
- Q71861823 P698 "8956050" @default.