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- Q56388262 description "article scientifique publié en 1993" @default.
- Q56388262 description "artículu científicu" @default.
- Q56388262 description "im Dezember 1993 veröffentlichter wissenschaftlicher Artikel" @default.
- Q56388262 description "wetenschappelijk artikel" @default.
- Q56388262 description "наукова стаття, опублікована в грудні 1993" @default.
- Q56388262 name "Cytogenetic survey of Apert syndrome. Reevaluation of a translocation (2;9)(p11.2;q34.2) in a patient suggests the breakpoints are not related to the disorder" @default.
- Q56388262 name "Cytogenetic survey of Apert syndrome. Reevaluation of a translocation" @default.
- Q56388262 type Item @default.
- Q56388262 label "Cytogenetic survey of Apert syndrome. Reevaluation of a translocation (2;9)(p11.2;q34.2) in a patient suggests the breakpoints are not related to the disorder" @default.
- Q56388262 label "Cytogenetic survey of Apert syndrome. Reevaluation of a translocation" @default.
- Q56388262 prefLabel "Cytogenetic survey of Apert syndrome. Reevaluation of a translocation (2;9)(p11.2;q34.2) in a patient suggests the breakpoints are not related to the disorder" @default.
- Q56388262 prefLabel "Cytogenetic survey of Apert syndrome. Reevaluation of a translocation" @default.
- Q56388262 P1433 Q56388262-09C31BC6-4882-413C-B3E0-6C98F41596B9 @default.
- Q56388262 P1476 Q56388262-732C6A98-0A7C-435B-AB31-FF4084FCC918 @default.
- Q56388262 P2093 Q56388262-05915383-867F-4767-BA57-3EA8A5BAEE28 @default.
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- Q56388262 P2093 Q56388262-46D9D624-5223-4807-9711-EAF1187B1637 @default.
- Q56388262 P2093 Q56388262-48BCD960-8C09-4727-9BE7-7A7D399BD77F @default.
- Q56388262 P2093 Q56388262-CC154AB6-8423-4BFE-87EE-862F21FE8B3C @default.
- Q56388262 P2093 Q56388262-D47517D3-B616-4F35-992B-3DF023DDA450 @default.
- Q56388262 P2093 Q56388262-E3ED3003-BF43-4130-A4D3-D2076945FB68 @default.
- Q56388262 P304 Q56388262-9536C7C4-0891-4636-9DA6-FD7B2266D9E1 @default.
- Q56388262 P31 Q56388262-689BCA4C-C7AA-4D61-82C8-1A401C88CB7A @default.
- Q56388262 P407 Q56388262-60E2599F-1031-4257-871B-1A19A0933A89 @default.
- Q56388262 P433 Q56388262-BF18083C-DBBC-4449-BB1F-BB8954AD64B2 @default.
- Q56388262 P478 Q56388262-E706C2B1-6F53-4C1F-9755-A78B6E71EE74 @default.
- Q56388262 P577 Q56388262-0D73FE50-9DBC-49E9-8A28-B9B68109A4A5 @default.
- Q56388262 P698 Q56388262-BE2B1847-8E12-40C6-89E8-C23AC79278FA @default.
- Q56388262 P698 8249950 @default.
- Q56388262 P1433 Q26839871 @default.
- Q56388262 P1476 "Cytogenetic survey of Apert syndrome. Reevaluation of a translocation (2;9)(p11.2;q34.2) in a patient suggests the breakpoints are not related to the disorder" @default.
- Q56388262 P2093 "A F Lewanda" @default.
- Q56388262 P2093 "E W Jabs" @default.
- Q56388262 P2093 "J Hood" @default.
- Q56388262 P2093 "J L Kennedy" @default.
- Q56388262 P2093 "M M Cohen" @default.
- Q56388262 P2093 "M Walters" @default.
- Q56388262 P2093 "S Morsey" @default.
- Q56388262 P304 "1306-8" @default.
- Q56388262 P31 Q13442814 @default.
- Q56388262 P407 Q1860 @default.
- Q56388262 P433 "12" @default.
- Q56388262 P478 "147" @default.
- Q56388262 P577 "1993-12-01T00:00:00Z" @default.
- Q56388262 P698 "8249950" @default.