Rezultati - Gecz Jozef
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1
TM4SF10 gene sequencing in XLMR patients identifies common polymorphisms but no disease-associated mutation od Holinski-Feder Elke, Abramowicz Marc J, Gecz Jozef, Kooy Frank, Christophe-Hobertus Christiane, Schwartz Charles, Christophe Daniel
Izdano 2004Signatura: Nalaganje...Connect to this object online.
Nahaja se: Nalaganje...
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2
A novel syndrome of paediatric cataract, dysmorphism, ectodermal features, and developmental delay in Australian Aboriginal family maps to 1p35.3-p36.32 od Gecz Jozef, Liebelt Jan E, Laurie Kate J, Hattersley Kathryn, Durkin Shane R, Craig Jamie E, Burdon Kathryn P
Izdano 2010Signatura: Nalaganje...Connect to this object online.
Nahaja se: Nalaganje...
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3
XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene od MacMillan Andrée, Macgregor David, Holinski-Feder Elke, Mangelsdorf Marie, Finnis Merran, Cason A Lauren, Stepp Monica L, Holden Jeanette JA, Gecz Jozef, Stevenson Roger E, Schwartz Charles E
Izdano 2005Signatura: Nalaganje...Connect to this object online.
Nahaja se: Nalaganje...
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