Confirmation of linkage of Clouston syndrome (hidrotic ectodermal dysplasia) to 13q11-q12.1 with Evidence for multiple independent mutations

Journal of Investigative Dermatology

Volumn 111, Issue 1, 1998, Pages 83-85

  Taylor, Todd D ^a   Hayflick, Susan J ^a,d   McKinnon, Wendy ^b   Guttmacher, Alan E ^b   Hovnanian, Alain ^c   Litt, Mike ^a   Zonana, Jonathan ^a  

^a OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^b UNIVERSITY OF VERMONT   (United States)

^c UNIVERSITY OF OXFORD   (United Kingdom)

^d Molecular and Medical Genetics   (United States)

Author keywords

Gene mapping; Hyperkeratosis; Microsatellite markers

Indexed keywords

ALLELE; ALOPECIA; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 13Q; CLINICAL ARTICLE; CLOUSTON SYNDROME; FEMALE; GENE FREQUENCY; GENE MUTATION; GENETIC LINKAGE; HAPLOTYPE; HUMAN; HYPOHIDROTIC ECTODERMAL DYSPLASIA; KERATOSIS PALMOPLANTARIS; MALE; NAIL DYSTROPHY; PRIORITY JOURNAL; SWEATING;

EID: 0031860399     PISSN: 0022202X     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1523-1747.1998.00245.x     Document Type: Article

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