Mutations of the homeobox gene MSX2 cause symmetric parietal foramina: contrasting effects of loss and gain of function mutations for skull development.
Wilkie Aom., Rob Maxson(University of Southern California), J A Hurst(Newcastle University), Krystyńa Chrzańowska(University Medical Center Groningen), Sonja Walsh, Asp Tang, Navaratnam Elanko, Richard L. Maas(Brigham and Women's Hospital), S A Wall(University Hospitals of Leicester NHS Trust), Twigg Srf.
The American Journal of Human Genetics
January 1, 1999
Cited by 1
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