The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference29 articles.
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5. A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval
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1. Long-Term Follow-Up of Dental Rehabilitation of a Patient with Clouston Syndrome and Congenital Edentulism (Issues of Theory and Clinical Practice);Medical University;2020-12-01
2. Ectodermal Dysplasias;Harper's Textbook of Pediatric Dermatology;2019-11-20
3. Mutation–proved Clouston syndrome in a large Indian family with a variant phenotype;Indian Journal of Dermatology;2019
4. Inherited Syndromes with Cutaneous Adnexal Neoplasms;Cutaneous Adnexal Neoplasms;2017
5. Identification of GJB6 gene mutation in an Indian man with Clouston syndrome;Indian Journal of Dermatology, Venereology, and Leprology;2016
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