Mutations of the homeobox gene MSX2 cause symmetric parietal foramina: contrasting effects of loss and gain of function mutations for skull development.

AOM Wilkie, A Tang, N Elanko,S Walsh,SRF Twigg, JA Hurst, K Chrzanowska,SA Wall, RL Maas, RE Maxson

AMERICAN JOURNAL OF HUMAN GENETICS(1999)

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