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- Q91111368 description "article scientifique publié en 2019" @default.
- Q91111368 description "artículu científicu espublizáu en xunu de 2019" @default.
- Q91111368 description "im Juni 2019 veröffentlichter wissenschaftlicher Artikel" @default.
- Q91111368 description "scientific article published on 01 June 2019" @default.
- Q91111368 description "wetenschappelijk artikel" @default.
- Q91111368 description "наукова стаття, опублікована 1 червня 2019" @default.
- Q91111368 name "A homozygous pathogenic missense variant broadens the phenotypic and mutational spectrum of CREB3L1-related osteogenesis imperfecta" @default.
- Q91111368 name "A homozygous pathogenic missense variant broadens the phenotypic and mutational spectrum of CREB3L1-related osteogenesis imperfecta" @default.
- Q91111368 type Item @default.
- Q91111368 label "A homozygous pathogenic missense variant broadens the phenotypic and mutational spectrum of CREB3L1-related osteogenesis imperfecta" @default.
- Q91111368 label "A homozygous pathogenic missense variant broadens the phenotypic and mutational spectrum of CREB3L1-related osteogenesis imperfecta" @default.
- Q91111368 prefLabel "A homozygous pathogenic missense variant broadens the phenotypic and mutational spectrum of CREB3L1-related osteogenesis imperfecta" @default.
- Q91111368 prefLabel "A homozygous pathogenic missense variant broadens the phenotypic and mutational spectrum of CREB3L1-related osteogenesis imperfecta" @default.
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- Q91111368 P1476 Q91111368-272F7336-2758-40BB-A9A4-DAFF09AC0225 @default.
- Q91111368 P2093 Q91111368-23BE4A52-A3A4-4337-BC41-4056878D5B38 @default.
- Q91111368 P2093 Q91111368-4E46148E-FC12-4526-BEA5-5EE70B719D57 @default.
- Q91111368 P2093 Q91111368-6040E250-0AEA-4FD9-B755-E0F7A041D385 @default.
- Q91111368 P2093 Q91111368-9059C4FC-07C3-4CB3-86AC-66F02807C8AA @default.
- Q91111368 P2093 Q91111368-94828EC8-A44C-4844-BB8C-7BAA4F3F2F42 @default.
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- Q91111368 P2860 Q91111368-0B32865F-29CB-4C03-8578-2AD480DF6073 @default.
- Q91111368 P304 Q91111368-F714C0F7-A011-4AF1-A979-A0AEBC102672 @default.
- Q91111368 P31 Q91111368-FDA938E7-DEA6-425A-ACB4-E6CA7A2D2DC6 @default.
- Q91111368 P356 Q91111368-30AB0E0C-257D-4F74-8806-3D1D9ECF28B9 @default.
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- Q91111368 P577 Q91111368-DE0EB450-B4AE-471A-9676-B148FC72BEE1 @default.
- Q91111368 P698 Q91111368-5A747386-4457-4A59-B520-011472FD3643 @default.
- Q91111368 P921 Q91111368-3534EA55-8681-4449-A8B1-7A488CC83D8D @default.
- Q91111368 P921 Q91111368-C0B2F5CD-44DD-47FC-975B-0BDB242897A8 @default.
- Q91111368 P356 DDZ017 @default.
- Q91111368 P698 30657919 @default.
- Q91111368 P1433 Q2720965 @default.
- Q91111368 P1476 "A homozygous pathogenic missense variant broadens the phenotypic and mutational spectrum of CREB3L1-related osteogenesis imperfecta" @default.
- Q91111368 P2093 "Anne De Paepe" @default.
- Q91111368 P2093 "Brecht Guillemyn" @default.
- Q91111368 P2093 "Delfien Syx" @default.
- Q91111368 P2093 "Fransiska Malfait" @default.
- Q91111368 P2093 "Hülya Kayserili" @default.
- Q91111368 P2093 "Lynn Demuynck" @default.
- Q91111368 P2093 "Paul J Coucke" @default.
- Q91111368 P2093 "Sofie Symoens" @default.
- Q91111368 P2860 Q29616810 @default.
- Q91111368 P304 "1801-1809" @default.
- Q91111368 P31 Q13442814 @default.
- Q91111368 P356 "10.1093/HMG/DDZ017" @default.
- Q91111368 P433 "11" @default.
- Q91111368 P478 "28" @default.
- Q91111368 P50 Q46217147 @default.
- Q91111368 P577 "2019-06-01T00:00:00Z" @default.
- Q91111368 P698 "30657919" @default.
- Q91111368 P921 Q114049690 @default.
- Q91111368 P921 Q749409 @default.