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Localisation of a gene for dominant cone-rod dystrophy (CORD6) to chromosome 17p.
Kelsell, R E; Evans, K; Gregory, C Y; Moore, A T; Bird, A C; Hunt, D M.
Affiliation
  • Kelsell RE; Department of Molecular Genetics, Institute of Ophthalmology, University College London, UK.
Hum Mol Genet ; 6(4): 597-600, 1997 Apr.
Article in En | MEDLINE | ID: mdl-9097965
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Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 17 / Retinitis Pigmentosa Type of study: Prognostic_studies Limits: Female / Humans / Male Country/Region as subject: Europa Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 1997 Document type: Article Affiliation country: United kingdom Country of publication: United kingdom
Search on Google
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 17 / Retinitis Pigmentosa Type of study: Prognostic_studies Limits: Female / Humans / Male Country/Region as subject: Europa Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 1997 Document type: Article Affiliation country: United kingdom Country of publication: United kingdom