TP63 gene mutation in ADULT syndrome
- 30 August 2001
- journal article
- case report
- Published by Springer Science and Business Media LLC in European Journal of Human Genetics
- Vol. 9 (8), 642-645
- https://doi.org/10.1038/sj.ejhg.5200676
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Heterozygous germline missense mutation in the p63 gene underlying EEC syndromeClinical and Experimental Dermatology, 2000
- Split-Hand/Split-Foot Malformation Is Caused by Mutations in the p63 Gene on 3q27American Journal of Human Genetics, 2000
- Adult syndrome allelic to limb mammary syndrome (LMS)?American Journal of Medical Genetics, 2000
- Heterozygous Germline Mutations in the p53 Homolog p63 Are the Cause of EEC SyndromeCell, 1999
- p63 is essential for regenerative proliferation in limb, craniofacial and epithelial developmentNature, 1999
- Limb Mammary Syndrome: A New Genetic Disorder with Mammary Hypoplasia, Ectrodactyly, and Other Hand/Foot Anomalies Maps to Human Chromosome 3q27American Journal of Human Genetics, 1999
- p63, a p53 Homolog at 3q27–29, Encodes Multiple Products with Transactivating, Death-Inducing, and Dominant-Negative ActivitiesMolecular Cell, 1998
- ADULT‐syndrome: An autosomal‐dominant disorder with pigment anomalies, ectrodactyly, nail dysplasia, and hypodontiaAmerican Journal of Medical Genetics, 1993