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- Q56332729 description "im November 2008 veröffentlichter wissenschaftlicher Artikel" @default.
- Q56332729 description "wetenschappelijk artikel" @default.
- Q56332729 description "наукова стаття, опублікована в листопаді 2008" @default.
- Q56332729 name "Cytogenetic and array CGH characterization of de novo 1p36 duplications and deletion in a patient with congenital cataracts, hearing loss, choanal atresia, and mental retardation" @default.
- Q56332729 name "Cytogenetic and array CGH characterization of de novo 1p36 duplications and deletion in a patient with congenital cataracts, hearing loss, choanal atresia, and mental retardation" @default.
- Q56332729 type Item @default.
- Q56332729 label "Cytogenetic and array CGH characterization of de novo 1p36 duplications and deletion in a patient with congenital cataracts, hearing loss, choanal atresia, and mental retardation" @default.
- Q56332729 label "Cytogenetic and array CGH characterization of de novo 1p36 duplications and deletion in a patient with congenital cataracts, hearing loss, choanal atresia, and mental retardation" @default.
- Q56332729 prefLabel "Cytogenetic and array CGH characterization of de novo 1p36 duplications and deletion in a patient with congenital cataracts, hearing loss, choanal atresia, and mental retardation" @default.
- Q56332729 prefLabel "Cytogenetic and array CGH characterization of de novo 1p36 duplications and deletion in a patient with congenital cataracts, hearing loss, choanal atresia, and mental retardation" @default.
- Q56332729 P1433 Q56332729-4E46DC5E-504F-463C-B7CE-95E5A690B65B @default.
- Q56332729 P1476 Q56332729-4591D268-2754-45AC-9CD2-ED4E4898AD0C @default.
- Q56332729 P2093 Q56332729-414E7182-D1E2-4729-A11A-84DF93E0CED1 @default.
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- Q56332729 P304 Q56332729-1F3D19A2-859D-4485-B515-DD3C943786A5 @default.
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- Q56332729 P407 Q56332729-2B23734B-0198-4B25-975C-385BBBB8585E @default.
- Q56332729 P433 Q56332729-1A768A6B-145C-4B12-8D29-B931B294B4E8 @default.
- Q56332729 P478 Q56332729-5A0D4E55-E515-4F3A-89CE-945AD4D02CC5 @default.
- Q56332729 P577 Q56332729-AD1136D6-5460-449C-891D-448AC5F80B20 @default.
- Q56332729 P698 Q56332729-55E1745A-C952-4760-97CD-23D135F0CCCD @default.
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- Q56332729 P921 Q56332729-FDEF5E64-E9B6-423A-8463-36592397409D @default.
- Q56332729 P356 AJMG.A.32437 @default.
- Q56332729 P698 18924166 @default.
- Q56332729 P1433 Q4744254 @default.
- Q56332729 P1476 "Cytogenetic and array CGH characterization of de novo 1p36 duplications and deletion in a patient with congenital cataracts, hearing loss, choanal atresia, and mental retardation" @default.
- Q56332729 P2093 "Elise Obolensky" @default.
- Q56332729 P2093 "Emily Chen" @default.
- Q56332729 P2093 "Katherine A Rauen" @default.
- Q56332729 P2093 "Lisa G Shaffer" @default.
- Q56332729 P2093 "Xu Li" @default.
- Q56332729 P304 "2785-90" @default.
- Q56332729 P31 Q13442814 @default.
- Q56332729 P356 "10.1002/AJMG.A.32437" @default.
- Q56332729 P407 Q1860 @default.
- Q56332729 P433 "21" @default.
- Q56332729 P478 "146A" @default.
- Q56332729 P577 "2008-11-01T00:00:00Z" @default.
- Q56332729 P698 "18924166" @default.
- Q56332729 P921 Q16035842 @default.
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