A homozygous BMPR1B mutation causes a new subtype of acromesomelic chondrodysplasia with genital anomalies | Journal of Medical Genetics

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

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Cite this article as:: Demirhan O, Türkmen S, Schwabe GC, et al

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

Journal of Medical Genetics 2005;42:314-317.