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- Q83161677 description "article scientifique publié en 2012" @default.
- Q83161677 description "artículu científicu espublizáu n'abril de 2012" @default.
- Q83161677 description "im April 2012 veröffentlichter wissenschaftlicher Artikel" @default.
- Q83161677 description "scientific article published on 01 April 2012" @default.
- Q83161677 description "wetenschappelijk artikel" @default.
- Q83161677 description "наукова стаття, опублікована у квітні 2012" @default.
- Q83161677 name "Apparent homozygosity for p.E1841K mutation in a patient with MYH9-related disorder: a misdiagnosis for an autosomal dominant disorder?" @default.
- Q83161677 name "Apparent homozygosity for p.E1841K mutation in a patient with MYH9-related disorder: a misdiagnosis for an autosomal dominant disorder?" @default.
- Q83161677 type Item @default.
- Q83161677 label "Apparent homozygosity for p.E1841K mutation in a patient with MYH9-related disorder: a misdiagnosis for an autosomal dominant disorder?" @default.
- Q83161677 label "Apparent homozygosity for p.E1841K mutation in a patient with MYH9-related disorder: a misdiagnosis for an autosomal dominant disorder?" @default.
- Q83161677 prefLabel "Apparent homozygosity for p.E1841K mutation in a patient with MYH9-related disorder: a misdiagnosis for an autosomal dominant disorder?" @default.
- Q83161677 prefLabel "Apparent homozygosity for p.E1841K mutation in a patient with MYH9-related disorder: a misdiagnosis for an autosomal dominant disorder?" @default.
- Q83161677 P1433 Q83161677-A50C0F31-610F-4573-B75B-F1864422CF7D @default.
- Q83161677 P1476 Q83161677-955FE1B4-1CC4-475D-B195-43C0B87B9338 @default.
- Q83161677 P2093 Q83161677-5927BA5E-AD8B-4A66-9795-41B16AC92F62 @default.
- Q83161677 P2093 Q83161677-94A6092B-1F30-404B-80BD-3027D2F7A327 @default.
- Q83161677 P2093 Q83161677-ADE1CFAE-5119-49D4-A3F0-81F3E0E91210 @default.
- Q83161677 P304 Q83161677-CC48BF49-1F3F-42A0-8093-326F33977B4F @default.
- Q83161677 P31 Q83161677-ECB1EBDE-4899-4CFD-89FD-27C3425139BE @default.
- Q83161677 P356 Q83161677-49EC8397-0E03-483A-B5EC-DC5F002F97A7 @default.
- Q83161677 P433 Q83161677-113DA4CD-709E-40E4-81FD-3165359A598A @default.
- Q83161677 P478 Q83161677-CA98503F-560E-40FF-9BF3-66A077A4FE43 @default.
- Q83161677 P577 Q83161677-B26EFF87-4A6A-4C90-BDA4-129C0A120CCB @default.
- Q83161677 P698 Q83161677-0B179519-1A20-49F5-8A0B-31F9B2C4238C @default.
- Q83161677 P921 Q83161677-02BBC385-CE20-43F5-BB1D-6EDA9EDFC93A @default.
- Q83161677 P921 Q83161677-6C8747A3-4AE6-4355-9CDB-523397BF632A @default.
- Q83161677 P921 Q83161677-A9EC2F05-9E93-49C4-9C61-032ED1F47C62 @default.
- Q83161677 P356 J.1600-0609.2011.01746.X @default.
- Q83161677 P698 22211851 @default.
- Q83161677 P1433 Q15765799 @default.
- Q83161677 P1476 "Apparent homozygosity for p.E1841K mutation in a patient with MYH9-related disorder: a misdiagnosis for an autosomal dominant disorder?" @default.
- Q83161677 P2093 "Béatrice Saposnik" @default.
- Q83161677 P2093 "Nicole Schlegel" @default.
- Q83161677 P2093 "Sylvie Binard" @default.
- Q83161677 P304 "365-366" @default.
- Q83161677 P31 Q13442814 @default.
- Q83161677 P356 "10.1111/J.1600-0609.2011.01746.X" @default.
- Q83161677 P433 "4" @default.
- Q83161677 P478 "88" @default.
- Q83161677 P577 "2012-04-01T00:00:00Z" @default.
- Q83161677 P698 "22211851" @default.
- Q83161677 P921 Q114049690 @default.
- Q83161677 P921 Q11631567 @default.
- Q83161677 P921 Q3843790 @default.