Identification of mutations in the MSX2 homeobox gene in families affected with foramina parietalia permagna.
Wuyts W; Reardon W; Preis S; Homfray T; Rasore-Quartino A; Christians H; Willems PJ; Van Hul W; Human Molecular Genetics, 2000, vol. 9, issue 8, p 1251, ISSN 09646906. ISBN 09646906.
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