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Clinically manifest X-linked recessive ichthyosis in a female due to a homozygous interstitial 1·6-Mb deletion of Xp22.31.
Nagtzaam, I F; Stegmann, A P A; Steijlen, P M; Herbergs, J; Van Lent-Albrechts, J A; Van Geel, M; Van Steensel, M A M.
Br J Dermatol ; 166(4): 905-7, 2012 Apr.
Article in En | MEDLINE | ID: mdl-21985695
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ichthyosis, X-Linked / Gene Deletion / Chromosomes, Human, X Limits: Adolescent / Female / Humans Language: En Journal: Br J Dermatol Year: 2012 Document type: Article Country of publication: Reino Unido
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ichthyosis, X-Linked / Gene Deletion / Chromosomes, Human, X Limits: Adolescent / Female / Humans Language: En Journal: Br J Dermatol Year: 2012 Document type: Article Country of publication: Reino Unido