A Gene for Autosomal Dominant Hypohidrotic Ectodermal Dysplasia (EDA3) Maps to Chromosome 2q11-q13-Reference-Cited by-同舟云学术

A Gene for Autosomal Dominant Hypohidrotic Ectodermal Dysplasia (EDA3) Maps to Chromosome 2q11-q13

Published:1998-05 Issue:5 Volume:62 Page:1102-1106
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Ho Lingling,Williams Marc S.,Spritz Richard A.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference12 articles.

1. Autosomal dominant hypohidrotic ectodermal dysplasia in a large family;Aswegan;Am J Med Genet,1997

2. Characterization of the the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development;Crackower;Hum Mol Genet,1996

3. Ectodermal dysplasias: a clinical and genetic study;Freire-Maia,1984

4. Ectodermal dysplasias: a review of the conditions described after 1984 with an overall analysis of all the conditions belonging to this nosologic group;Freire-Maia;Rev Bras Genet,1987

5. Hypohidrotic ectodermal dysplasia in females: a critical analysis and argument for genetic heterogeneity;Gorlin;Z Kinderheilkd,1970

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