Clinical variation in X-linked dominant chondrodysplasia punctata (X-linked dominant ichthyosis).

Feldmeyer, L; Mevorah, B; Grzeschik, K H; Huber, M; Hohl, D

Feldmeyer, L; Mevorah, B; Grzeschik, K H; Huber, M; Hohl, D.

Affiliation

Feldmeyer L; Institute of Cell Biology, ETH Hönggerberg, Zürich, Switzerland. laurence.feldmeyer@cell.biol.ethz.ch

Br J Dermatol ; 154(4): 766-9, 2006 Apr.

Article in En | MEDLINE | ID: mdl-16536827

Subject(s)

Chondrodysplasia Punctata/genetics; Ichthyosis, X-Linked/genetics; Adult; Base Sequence; Chondrodysplasia Punctata/pathology; Female; Frameshift Mutation; Humans; Ichthyosis, X-Linked/pathology; Infant, Newborn; Steroid Isomerases/genetics

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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Chondrodysplasia Punctata / Ichthyosis, X-Linked Limits: Adult / Female / Humans / Newborn Language: En Journal: Br J Dermatol Year: 2006 Document type: Article

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