A Gene for Autosomal Dominant Hypohidrotic Ectodermal Dysplasia (EDA3) Maps to Chromosome 2q11-q13
- 1 May 1998
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 62 (5) , 1102-1106
- https://doi.org/10.1086/301839
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
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- X–linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane proteinNature Genetics, 1996
- Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb developmentHuman Molecular Genetics, 1996
- The gene responsible for Clouston hidrotic ectodermal dysplasia maps to the pericentromeric region of chromosome 13qHuman Molecular Genetics, 1996
- EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) is on 7p11.2‐q21.3Clinical Genetics, 1992
- EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) with a balanced reciprocal translocation between 7q11.21 and 9p12 (or 7p11.2 and 9q12) in three generationsClinical Genetics, 1991
- AUTOSOMAL DOMINANT ECTODERMAL DYSPLASIA1987