We don’t have enough information about this author to calculate their statistics. If you think this is an error let us know.
Learn More
The trichorhinophalangeal syndrome type I is a rare, probably autosomal-dominant inherited disorder, characterized by anomalies of the cranium and face, hair, skeleton and soft parts of the hands and the feet. Typical deformities of the syndrome in hands and feet (e.g. brachydactylie, deviation and curvature of fingers and toes due to cone-shaped joints)(More)
  • 1