Publication | Open Access
Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate
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Citations
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References
2016
Year
Developmental AnomalyDevelopmental BiologyGenetic DisorderMedicineGeneticsCraniofacial AnomaliesNonsyndromic Cleft PalateMolecular GeneticsGenomicsMolecular DiagnosticsCommon Susceptibility VariantVariant InterpretationCleft Lip
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