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- Q84936942 description "article scientifique publié en 2011" @default.
- Q84936942 description "artículu científicu espublizáu en setiembre de 2011" @default.
- Q84936942 description "im September 2011 veröffentlichter wissenschaftlicher Artikel" @default.
- Q84936942 description "scientific article published on 09 September 2011" @default.
- Q84936942 description "wetenschappelijk artikel" @default.
- Q84936942 description "наукова стаття, опублікована у вересні 2011" @default.
- Q84936942 description "գիտական հոդված հրատարակված 2011 թվականի սեպտեմբերի 9-ին" @default.
- Q84936942 name "X-linked VACTERL with hydrocephalus syndrome: further delineation of the phenotype caused by FANCB mutations" @default.
- Q84936942 name "X-linked VACTERL with hydrocephalus syndrome: further delineation of the phenotype caused by FANCB mutations" @default.
- Q84936942 type Item @default.
- Q84936942 label "X-linked VACTERL with hydrocephalus syndrome: further delineation of the phenotype caused by FANCB mutations" @default.
- Q84936942 label "X-linked VACTERL with hydrocephalus syndrome: further delineation of the phenotype caused by FANCB mutations" @default.
- Q84936942 prefLabel "X-linked VACTERL with hydrocephalus syndrome: further delineation of the phenotype caused by FANCB mutations" @default.
- Q84936942 prefLabel "X-linked VACTERL with hydrocephalus syndrome: further delineation of the phenotype caused by FANCB mutations" @default.
- Q84936942 P1433 Q84936942-8FC84B63-AE6E-472E-A2AA-382F449F87E1 @default.
- Q84936942 P1476 Q84936942-5B859221-44C5-490A-BF48-F3016770D5E1 @default.
- Q84936942 P2093 Q84936942-035B44AA-91EB-4E42-BCEE-5614D59FA2B3 @default.
- Q84936942 P2093 Q84936942-2E143FB5-ED14-4C2B-A6CF-A3803E24DF3C @default.
- Q84936942 P2093 Q84936942-405ECB13-F357-44AE-92F5-A3F3C9A9445F @default.
- Q84936942 P2093 Q84936942-466C7873-4073-47C2-BD44-2C2DAC611DA0 @default.
- Q84936942 P2093 Q84936942-97455F06-0E94-46C9-A67A-ADBF66558451 @default.
- Q84936942 P2093 Q84936942-9D00877C-EFB8-4AC0-9DDC-FA337B70FCF1 @default.
- Q84936942 P2093 Q84936942-E4D002C8-EB24-40DA-A0B5-D6D31E6E34BC @default.
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- Q84936942 P2093 Q84936942-F99007D7-664D-4D77-9FC9-7D552779059D @default.
- Q84936942 P304 Q84936942-11D6091C-F191-424E-BE9B-DA52492B6DCF @default.
- Q84936942 P31 Q84936942-CDE67A91-26BE-400E-B050-54266A24795A @default.
- Q84936942 P356 Q84936942-158AF135-8AC0-4FF3-A9D6-47814E0D2510 @default.
- Q84936942 P433 Q84936942-A08012B5-FC26-4739-855F-90B1FD30576B @default.
- Q84936942 P478 Q84936942-93AA5097-42E9-41AB-98D2-9DB3300065BA @default.
- Q84936942 P50 Q84936942-4B9BA410-8D8E-487D-8E14-14E96BA9162C @default.
- Q84936942 P577 Q84936942-09ED2C60-8EB1-4C8E-9D0D-CD77F29163C0 @default.
- Q84936942 P698 Q84936942-635E4F2C-86DC-4CC0-86FA-3FD11C9BDF45 @default.
- Q84936942 P921 Q84936942-5A4F8AA5-D4C8-4DF2-BC53-8D2AA2055510 @default.
- Q84936942 P921 Q84936942-D8B1552D-EEA8-4D8C-A42E-77A2342B8996 @default.
- Q84936942 P356 AJMG.A.33913 @default.
- Q84936942 P698 21910217 @default.
- Q84936942 P1433 Q4744254 @default.
- Q84936942 P1476 "X-linked VACTERL with hydrocephalus syndrome: further delineation of the phenotype caused by FANCB mutations" @default.
- Q84936942 P2093 "Alasdair Hunter" @default.
- Q84936942 P2093 "Fiona Vaz" @default.
- Q84936942 P2093 "Jeremy Robertson" @default.
- Q84936942 P2093 "Joanna McCauley" @default.
- Q84936942 P2093 "Kate Gibson" @default.
- Q84936942 P2093 "Navta Masand" @default.
- Q84936942 P2093 "Ruth McGowan" @default.
- Q84936942 P2093 "Simon T Holden" @default.
- Q84936942 P2093 "Stephen Abbs" @default.
- Q84936942 P2093 "Sulekha Rajagopalan" @default.
- Q84936942 P304 "2370-2380" @default.
- Q84936942 P31 Q13442814 @default.
- Q84936942 P356 "10.1002/AJMG.A.33913" @default.
- Q84936942 P433 "10" @default.
- Q84936942 P478 "155A" @default.
- Q84936942 P50 Q102286139 @default.
- Q84936942 P577 "2011-09-09T00:00:00Z" @default.
- Q84936942 P698 "21910217" @default.
- Q84936942 P921 Q104053 @default.
- Q84936942 P921 Q55999486 @default.