Three successive generations of women with anhidrotic/hypohidrotic ectodermal dysplasia.

EDAR mutation in autosomal dominant hypohidrotic ectodermal dysplasia in two Swedish families. BMC Med Genet (2006) 0.95

EDAR-induced hypohidrotic ectodermal dysplasia: a clinical study on signs and symptoms in individuals with a heterozygous c.1072C > T mutation. BMC Med Genet (2014) 0.82

X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein. Nat Genet (1996) 3.90

Ectodermal dysplasias: a clinical classification and a causal review. Am J Med Genet (1994) 3.09

Hypohidrotic ectodermal dysplasia. J Med Genet (1987) 1.83

Permanent correction of an inherited ectodermal dysplasia with recombinant EDA. Nat Med (2003) 1.75

Ectodermal dysplasias: a new clinical-genetic classification. J Med Genet (2001) 1.58

Clinical spectrum of anhidrotic ectodermal dysplasia. Arch Dermatol (1970) 1.49

Ectodermal dysplasias: not only 'skin' deep. Clin Genet (2000) 1.04

Anhidrotic ectodermal dysplasia and immunodeficiency: the role of NEMO. Arch Dis Child (2003) 0.96

Both recessive and dominant forms of anhidrotic/hypohidrotic ectodermal dysplasia map to chromosome 2q11-q13. Am J Hum Genet (1999) 0.94