Publication | Closed Access
A Locus in 2p13–p14 (OFC2), in Addition to That Mapped in 6p23, Is Involved in Nonsyndromic Familial Orofacial Cleft Malformation
54
Citations
36
References
1998
Year
Developmental AnomalyChromatinDevelopmental BiologyGenetic DisorderGeneticsCraniofacial AnomaliesCraniofacial DevelopmentPathologyCleft Lip RepairMolecular GeneticsMedicineCraniofacial DisorderCleft Lip
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