Disease: Acro Dermato Ungual Lacrimal Tooth Syndrome
- 'Double trouble': diagnostic challenges in genetic skin disorders
- A novel c.1037C > G (p.Ala346Gly) mutation in TP63 as cause of the ectrodactyly-ectodermal dysplasia and cleft lip/palate (EEC) syndrome
- 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>
- Acro-dermato-ungual-lacrimal-tooth (ADULT) syndrome: report of a child with phenotypic overlap with ulnar-mammary syndrome and a new mutation in TP63
- Acro-Dermato-Ungual-Lacrimal-Tooth Syndrome: An Uncommon Member of the Ectodermal Dysplasias
- Acro-dermato-ungual-lacrimal-tooth syndrome: case report
- Acro-dermato-ungual-lacrimal-tooth-like syndrome: report of a family with variable expression
- ADULT (acro-dermato-ungual-lacrimal-tooth) Syndrome: A Case Report from India
- ADULT ectodermal dysplasia syndrome resulting from the missense mutation R298Q in the p63 gene
- ADULT Phenotype and rs16864880 in the <em>TP63</em> Gene: Two New Cases and Review of the Literature
- ADULT syndrome allelic to limb mammary syndrome (LMS)?
- ADULT syndrome caused by a mutation previously associated with EEC syndrome
- ADULT syndrome due to an R243W mutation in TP63
- ADULT syndrome: dental features of a very rare condition
- ADULT syndrome: phenotype in a Brazilian family with the R298Q mutation
- ADULT-syndrome: an autosomal-dominant disorder with pigment anomalies, ectrodactyly, nail dysplasia, and hypodontia
- Cerebral hemorrhage caused by shaking adult syndrome? Evidence from biomechanical analysis using 3D motion capture and finite element models
- Cleft palate and ADULT phenotype in a patient with a novel TP63 mutation suggests lumping of EEC/LM/ADULT syndromes into a unique entity: ELA syndrome
- Delineation of the ADULT syndrome phenotype due to arginine 298 mutations of the p63 gene
- Ectodermal dysplasias: the p63 tail
- EEC- and ADULT-associated TP63 mutations exhibit functional heterogeneity toward P63 responsive sequences
- EEC-LM-ADULT syndrome caused by R319H mutation in TP63 with ectrodactyly, syndactyly, and teeth anomaly: A case report
- Functional characterization of a novel TP63 mutation in a family with overlapping features of Rapp-Hodgkin/AEC/ADULT syndromes
- Further phenotypic and genetic variation in ADULT syndrome
- Gain-of-function mutation in ADULT syndrome reveals the presence of a second transactivation domain in p63
- Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63
- Human hepatic distomatosis (due to Fasciola hepatica;) 3 observations in children and one in an adult. Syndrome of anicteric acute hepatitis with massive eosinophilia; clinical and epidemiologic studies
- Intermediate Phenotype between ADULT Syndrome and EEC Syndrome Caused by R243Q Mutation in TP63
- Mutation analysis of p63 gene in the first Chinese family with ADULT syndrome
- p63 gene analysis in Mexican patients with syndromic and non-syndromic ectrodactyly
- P63 gene mutations and human developmental syndromes
- Prenatal diagnosis of acro-dermatoungual-lacrimal-tooth syndrome, a dominantly inherited ectrodactyly
- Shaken adult syndrome due to ocean wave: an autopsy case
- The Hay Wells syndrome-derived TAp63alphaQ540L mutant has impaired transcriptional and cell growth regulatory activity
- Unusual manifestations of ectodermal dysplasia-syndactyly syndrome type I in two Yemeni siblings