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- Q81346770 description "artículu científicu espublizáu en payares de 2005" @default.
- Q81346770 description "im November 2005 veröffentlichter wissenschaftlicher Artikel" @default.
- Q81346770 description "scientific article published on 01 November 2005" @default.
- Q81346770 description "wetenschappelijk artikel" @default.
- Q81346770 description "наукова стаття, опублікована в листопаді 2005" @default.
- Q81346770 name "A novel 17 bp deletion in the PHOX2B gene causes congenital central hypoventilation syndrome with total aganglionosis of the small and large intestine" @default.
- Q81346770 name "A novel 17 bp deletion in the PHOX2B gene causes congenital central hypoventilation syndrome with total aganglionosis of the small and large intestine" @default.
- Q81346770 type Item @default.
- Q81346770 label "A novel 17 bp deletion in the PHOX2B gene causes congenital central hypoventilation syndrome with total aganglionosis of the small and large intestine" @default.
- Q81346770 label "A novel 17 bp deletion in the PHOX2B gene causes congenital central hypoventilation syndrome with total aganglionosis of the small and large intestine" @default.
- Q81346770 prefLabel "A novel 17 bp deletion in the PHOX2B gene causes congenital central hypoventilation syndrome with total aganglionosis of the small and large intestine" @default.
- Q81346770 prefLabel "A novel 17 bp deletion in the PHOX2B gene causes congenital central hypoventilation syndrome with total aganglionosis of the small and large intestine" @default.
- Q81346770 P1433 Q81346770-C1DF79B8-F8F3-488C-B660-8B744A532AAC @default.
- Q81346770 P1476 Q81346770-527CA1D1-847C-4007-81F8-B4C10F41CE62 @default.
- Q81346770 P2093 Q81346770-3A132A9E-D241-4C56-AC61-D4BB8F3DBE50 @default.
- Q81346770 P2093 Q81346770-3DD05AB0-512A-49A8-8924-B53E62C7A056 @default.
- Q81346770 P2093 Q81346770-3E22D8D5-A916-439C-A1BD-4098BF450FB1 @default.
- Q81346770 P2093 Q81346770-4E07E094-141A-4D0A-8D2F-34CCC9FDBD87 @default.
- Q81346770 P2093 Q81346770-927837CD-5BF7-4D53-89B6-BBDC76253906 @default.
- Q81346770 P2093 Q81346770-9F9217E1-872A-402C-ACB3-82F38308DA28 @default.
- Q81346770 P2093 Q81346770-D6AAB5EB-38C4-49C4-8D45-9F5325F552C5 @default.
- Q81346770 P2093 Q81346770-F7CB04A9-0F3B-4D71-AAE4-308212E2693F @default.
- Q81346770 P304 Q81346770-845DFF17-8B4A-493A-ABD7-B62109B7FC19 @default.
- Q81346770 P31 Q81346770-9C5C9D77-384E-42F0-9C43-AFE5F271E41D @default.
- Q81346770 P356 Q81346770-A7E79848-6397-4FCB-B14F-EC237631CD84 @default.
- Q81346770 P433 Q81346770-18948DBF-491A-45BF-81F6-FF88EB0367D9 @default.
- Q81346770 P478 Q81346770-C4573022-11B0-4F67-91AD-3EA8E32B38D9 @default.
- Q81346770 P577 Q81346770-0AF32B2D-999A-4809-A3B6-6122C3DABB63 @default.
- Q81346770 P698 Q81346770-00F7F792-1ED9-4EDB-8448-8C58B57ACD27 @default.
- Q81346770 P921 Q81346770-481E4E70-D56E-45D5-B728-CAD4EF371E57 @default.
- Q81346770 P356 AJMG.A.30975 @default.
- Q81346770 P698 16222683 @default.
- Q81346770 P1433 Q4744254 @default.
- Q81346770 P1476 "A novel 17 bp deletion in the PHOX2B gene causes congenital central hypoventilation syndrome with total aganglionosis of the small and large intestine" @default.
- Q81346770 P2093 "Andreas Holzinger" @default.
- Q81346770 P2093 "Hans-Georg Münch" @default.
- Q81346770 P2093 "Helga Priessmann" @default.
- Q81346770 P2093 "Holger Till" @default.
- Q81346770 P2093 "Markus Hammel" @default.
- Q81346770 P2093 "Rashmi A Mittal" @default.
- Q81346770 P2093 "Stephan Ihrler" @default.
- Q81346770 P2093 "Walter Kachel" @default.
- Q81346770 P304 "50-51" @default.
- Q81346770 P31 Q13442814 @default.
- Q81346770 P356 "10.1002/AJMG.A.30975" @default.
- Q81346770 P433 "1" @default.
- Q81346770 P478 "139" @default.
- Q81346770 P577 "2005-11-01T00:00:00Z" @default.
- Q81346770 P698 "16222683" @default.
- Q81346770 P921 Q979129 @default.