Negative-configuration electroretinogram in Oregon eye disease. Consistent phenotype in Xp21 deletion syndrome.

Pillers, D A; Seltzer, W K; Powell, B R; Ray, P N; Tremblay, F; La Roche, G R; Lewis, R A; McCabe, E R; Eriksson, A W; Weleber, R G

Pillers, D A; Seltzer, W K; Powell, B R; Ray, P N; Tremblay, F; La Roche, G R; Lewis, R A; McCabe, E R; Eriksson, A W; Weleber, R G.

Affiliation

Pillers DA; Department of Pediatrics, Children's Hospital, Oregon Health Sciences University, Portland.

Arch Ophthalmol ; 111(11): 1558-63, 1993 Nov.

Article in En | MEDLINE | ID: mdl-8240114

Subject(s)

Albinism, Ocular/genetics; Chromosome Aberrations/genetics; Chromosome Deletion; Glycerol Kinase/genetics; Muscular Dystrophies/genetics; X Chromosome; Adolescent; Albinism, Ocular/physiopathology; Child; Child, Preschool; Chromosome Aberrations/physiopathology; Chromosome Disorders; Electroretinography; Glycerol Kinase/deficiency; Humans; Male; Muscular Dystrophies/enzymology; Muscular Dystrophies/physiopathology; Phenotype; Retina/physiology; Syndrome

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Collection: 01-internacional Database: MEDLINE Main subject: X Chromosome / Albinism, Ocular / Chromosome Aberrations / Chromosome Deletion / Glycerol Kinase / Muscular Dystrophies Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Child / Child, preschool / Humans / Male Language: En Journal: Arch Ophthalmol Year: 1993 Document type: Article

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