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DECIPHER: database for the interpretation of phenotype-linked plausibly pathogenic sequence and copy-number variation.
Bragin, Eugene; Chatzimichali, Eleni A; Wright, Caroline F; Hurles, Matthew E; Firth, Helen V; Bevan, A Paul; Swaminathan, G Jawahar.
Affiliation
  • Bragin E; Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SD, UK and Cambridge University Department of Medical Genetics, Addenbrooke's Hospital, Cambridge CB2 2QQ, UK.
Nucleic Acids Res ; 42(Database issue): D993-D1000, 2014 Jan.
Article in En | MEDLINE | ID: mdl-24150940
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Databases, Nucleic Acid / DNA Copy Number Variations / Genotype Type of study: Prognostic_studies Limits: Humans Language: En Journal: Nucleic Acids Res Year: 2014 Document type: Article Affiliation country: Reino Unido Country of publication: Reino Unido
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Databases, Nucleic Acid / DNA Copy Number Variations / Genotype Type of study: Prognostic_studies Limits: Humans Language: En Journal: Nucleic Acids Res Year: 2014 Document type: Article Affiliation country: Reino Unido Country of publication: Reino Unido