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A mutation in the receptor binding site of GDF5 causes Mohr-Wriedt brachydactyly type A2
Authors: Kjaer, K. W.; Eiberg, H.; Hansen, L.; van der Hagen, C. B.; Rosendahl, K.; Tommerup, N.; Mundlos, S.
Date of Publication (YYYY-MM-DD): 2006-03
Title of Journal: Journal of Medical Genetics (London)
Volume: 43
Issue / Number: 3
Start Page: 225
End Page: 231
Document Type: Article
ID: 313087.0