Definitive Evidence for an Autosomal Recessive Form of Hypohidrotic Ectodermal Dysplasia Clinically Indistinguishable rom the More Common X-Linked Disorde-Reference-Cited by-同舟云学术

Definitive Evidence for an Autosomal Recessive Form of Hypohidrotic Ectodermal Dysplasia Clinically Indistinguishable rom the More Common X-Linked Disorde

Published:1997-07 Issue:1 Volume:61 Page:94-100
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Munoz R.,Lestringant G.,Sybert V.,Frydman M.,Alswaini A.,Frossard P.M.,Jorgenson R.,Zonana J.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference24 articles.

1. Autosomal recessive anhidrotic ectodermal dysplasia: report of a case and discrimination of diagnostic features;Anton-Lamprecht;Birth Defects,1988

2. Anhidrosis and absence of sweat glands in mice hemizygous for the Tabby gene: supportive evidence for the hypothesis of homology between Tabby and human anhidrotic (hypohidrotic) ectodermal dysplasia (Christ-Siemens-Touraine syndrome);Blecher;J Invest Dermatol,1986

3. Dinucleotide repeat polymorphism at the XXS1111 locus;Browne;Hum Mol Genet,1993

4. Clinical aspects of X-linked hypohidrotic ectodermal dysplasia;Clarke;Arch Dis Child,1987

5. Hypohidrotic ectodermal dysplasia: a study of sweat pores in the X-linked form and in a family with probable autosomal recessive inheritance;Crump;J Pediatr,1971

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