Publication | Closed Access
Limbal Stem Cell Deficiency and Ocular Phenotype in Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome Caused by p63 Mutations
109
Citations
34
References
2011
Year
Developmental AnomalyDevelopmental BiologyOcular PhenotypeOphthalmologyEctrodactyly-ectodermal Dysplasia-clefting SyndromeGenetic DisorderGeneticsCraniofacial AnomaliesMedicineCraniofacial DisorderCleft LipP63 Mutations
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