Disease: Ectrodactyly-ectodermal dysplasia-cleft lip/cleft palate
- <em>TP63</em>-Related Disorders
- A novel mutation (c.1010G>T; p.R337L) in TP63 as a cause of split-hand/foot malformation with hypodontia
- A spectrum of TP63-related disorders with eight affected individuals in five unrelated families
- Absent meibomian glands and cone dystrophy in ADULT syndrome: identification by whole exome sequencing of pathogenic variants in two causal genes <em>TP63</em> and <em>CNGB3</em>
- Case report: Prenatal diagnosis of Ectrodactyly-Ectodermal dysplasia-Cleft syndrome (EEC) in a fetus with cleft lip and polycystic kidney
- Dental management of a child with ectrodactyly ectodermal dysplasia cleft lip/palate syndrome: A case report
- Ectodermal dysplasia and cholesteatoma: A cross-sectional analysis of otologic issues
- Ectrodactyly ectodermal dysplasia-cleft lip/palate syndrome: a case report
- Ectrodactyly-Ectodermal Dysplasia-Cleft Syndrome: Ocular Findings and Surgical Treatment
- EEC-LM-ADULT syndrome caused by R319H mutation in TP63 with ectrodactyly, syndactyly, and teeth anomaly: A case report
- Evolution of Acquired Middle Ear Cholesteatoma in Patients With Ectrodactyly, Ectodermal Dysplasia, Cleft Lip/Palate (EEC) Syndrome
- Expanding the phenotypic spectrum of TP63-related disorders including the first set of monozygotic twins
- Identification of a Tp63 gene variant in an abortus with Ectrodactyly, Ectodermal dysplasia, Cleft lip/palate syndrome by whole-exome sequencing
- Infrared meibography and molecular assessment of p63 gene mutations in a Mexican patient with EEC syndrome
- Management of Severely Atrophic Maxilla in Ectrodactyly Ectodermal Dysplasia-cleft Syndrome
- Peripheral giant cell granuloma in a child with ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome: a case report
- Prevalence rates for ectodermal dysplasia syndromes
- Prosthetic rehabilitation of a patient with ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome through a hybrid workflow: A case report with 2-year follow-up
- Sweating ability of patients with p63-associated syndromes
- Tooth defects of EEC and AEC syndrome caused by heterozygous TP63 mutations in three Chinese families and genotype-phenotype correlation analyses of TP63-related disorders