Author:
Klopocki Eva,Hennig Bianca P.,Dathe Katarina,Koll Randi,de Ravel Thomy,Baten Emiel,Blom Eveline,Gillerot Yves,Weigel Johannes F.W.,Krüger Gabriele,Hiort Olaf,Seemann Petra,Mundlos Stefan
Subject
Genetics (clinical),Genetics
Reference34 articles.
1. The brachydactylies: A molecular disease family;Mundlos;Clin. Genet.,2009
2. Brachydactyly and mental retardation: An Albright hereditary osteodystrophy-like syndrome localized to 2q37;Wilson;Am. J. Hum. Genet.,1995
3. Missense mutations in the homeodomain of HOXD13 are associated with brachydactyly types D and E;Johnson;Am. J. Hum. Genet.,2003
4. Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tract;Goodman;Proc. Natl. Acad. Sci. USA,1997
5. Analysis of the GNAS1 gene in Albright's hereditary osteodystrophy;Ahrens;J. Clin. Endocrinol. Metab.,2001
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