Chondrodysplasia punctata: case report and review of audiological and ENT features.

Murdin, L; Sirimanna, T; Hartley, B E; Holder, S E

Murdin, L; Sirimanna, T; Hartley, B E; Holder, S E.

Affiliation

Murdin L; Department of Audiology, Great Ormond Street Hospital for Sick Children, London, UK. louisa@murdin.com

J Laryngol Otol ; 120(3): 233-6, 2006 Mar.

Article in En | MEDLINE | ID: mdl-16359148

Subject(s)

Chondrodysplasia Punctata/pathology; Bronchoscopy; Chondrodysplasia Punctata/genetics; Chondrodysplasia Punctata/physiopathology; Genes, X-Linked/genetics; Humans; Infant; Laryngoscopy; Larynx/pathology; Male; Phenotype

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Collection: 01-internacional Database: MEDLINE Main subject: Chondrodysplasia Punctata Limits: Humans / Infant / Male Language: En Journal: J Laryngol Otol Journal subject: OTORRINOLARINGOLOGIA Year: 2006 Type: Article Affiliation country: United kingdom

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