Disease: Ectodermal dysplasia ectrodactyly macular dystrophy
- Association of ectodermal dysplasia, ectrodactyly and macular dystrophy: EEM syndrome (case report)
- Association of ectodermal dysplasia, ectrodactyly, and macular dystrophy: the EEM syndrome
- CDH3-Related Syndromes: Report on a New Mutation and Overview of the Genotype-Phenotype Correlations
- Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome)
- Ectodermal dysplasia-ectrodactyly-macular dystrophy
- Ectodermal dysplasia, ectrodactyly and macular dystrophy (EEM syndrome) in siblings
- Ectrodactyly, ectodermal dysplasia, macular degeneration syndrome: a further contribution
- EEM syndrome: report of a family and results of a ten-year follow-up
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Ophthalmological findings in ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome: a case report
- P-cadherin is a p63 target gene with a crucial role in the developing human limb bud and hair follicle
- Splice site mutations in the P-cadherin gene underlie hypotrichosis with juvenile macular dystrophy
- The first reported case of <em>CDH3</em>-related hypotrichosis with juvenile macular dystrophy from Jordan: a case report
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle