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A homozygous BMPR1B mutation causes a new subtype of acromesomelic chondrodysplasia with genital anomalies
- Correspondence to: Stefan Mundlos Institut für Medizinische Genetik, Universitätsmedizin Berlin, Charité, Augustenburger Platz 1, 13353 Berlin, Germany; stefan.mundloscharite.de
Citation
A homozygous BMPR1B mutation causes a new subtype of acromesomelic chondrodysplasia with genital anomalies
Publication history
- Accepted July 6, 2004
- Revised July 2, 2004
- First published April 1, 2005.
Online issue publication
April 27, 2016
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Copyright 2005 Journal of Medical Genetics