Kjaer, K. W., H. Eiberg, L. Hansen, C. B. van der Hagen, K. Rosendahl, N. Tommerup and S. Mundlos: A mutation in the receptor binding site of GDF5 causes Mohr-Wriedt brachydactyly type A2. In: Journal of Medical Genetics (London) 43, 3, 225-231 (2006).
doi: 10.1136/jmg.2005.034058
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