A founder mutation for ichthyosis prematurity syndrome restricted to 76 kb by haplotype association.

Melin, M; Klar, J; Jr Gedde-Dahl, T; Fredriksson, R; Hausser, I; Brandrup, F; Bygum, A; Vahlquist, A; Hellström Pigg, M; Dahl, N

Melin, M; Klar, J; Jr Gedde-Dahl, T; Fredriksson, R; Hausser, I; Brandrup, F; Bygum, A; Vahlquist, A; Hellström Pigg, M; Dahl, N.

Affiliation

Melin M; Department of Genetics and Pathology, Rudbeck Laboratory, Uppsala University, Uppsala, 751 85, Sweden.
Klar J; Department of Genetics and Pathology, Rudbeck Laboratory, Uppsala University, Uppsala, 751 85, Sweden.
Jr Gedde-Dahl T; Department of Dermatology, Rikshospitalet University Hospital, and Institute of Forensic Medicine, University of Oslo, Oslo, Norway.
Fredriksson R; Department of Neuroscience, Uppsala University, Uppsala, Sweden.
Hausser I; Department of Dermatology, University of Heidelberg, Heidelberg, Germany.
Brandrup F; Department of Dermatology, Odense University Hospital, Odense, Denmark.
Bygum A; Department of Dermatology, Odense University Hospital, Odense, Denmark.
Vahlquist A; Department of Medical Science, Uppsala University Hospital, Uppsala, Sweden.
Hellström Pigg M; Department of Genetics and Pathology, Rudbeck Laboratory, Uppsala University, Uppsala, 751 85, Sweden.
Dahl N; Department of Genetics and Pathology, Rudbeck Laboratory, Uppsala University, Uppsala, 751 85, Sweden. niklas.dahl@genpat.uu.se.

J Hum Genet ; 51(10): 864-871, 2006.

Article in En | MEDLINE | ID: mdl-16946994

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Founder Effect / Ichthyosis / Mutation Type of study: Risk_factors_studies Limits: Humans Country/Region as subject: Europa Language: En Journal: J Hum Genet Journal subject: GENETICA MEDICA Year: 2006 Document type: Article Affiliation country: Suecia

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