A homozygous BMPR1B mutation causes a new subtype of acromesomelic chondrodysplasia with genital anomalies

Por Demirhan, O, Turkmen, S, Schwabe, G, Soyupak, S, Akgul, E, Tastemir, D, Karahan, D, Mundlos, S, Lehmann, K
Publicado em 2005