A man, a syndrome, a gene: Clouston's hidrotic ectodermal dysplasia (HED)
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference10 articles.
1. The gene responsible for Clouston hidrotic ectodermal dysplasia maps to the pericentromeric region of chromosome 13q
2. A Radiation Hybrid Map of 48 Loci Including the Clouston Hidrotic Ectodermal Dysplasia Locus in the Pericentromeric Region of Chromosome 13q
3. Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping
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2. Mutant Cx30-A88V mice exhibit hydrocephaly and sex-dependent behavioral abnormalities, implicating a functional role for Cx30 in the brain;Disease Models & Mechanisms;2021-01-01
3. 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
4. The connexin30 A88V mutant reduces cochlear gap junction expression and confers long-term protection against hearing loss;Journal of Cell Science;2018-01-01
5. Ectodermal Dysplasias;Rook's Textbook of Dermatology, Ninth Edition;2016-10-09
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