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Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability.
Grozeva, Detelina; Carss, Keren; Spasic-Boskovic, Olivera; Tejada, Maria-Isabel; Gecz, Jozef; Shaw, Marie; Corbett, Mark; Haan, Eric; Thompson, Elizabeth; Friend, Kathryn; Hussain, Zaamin; Hackett, Anna; Field, Michael; Renieri, Alessandra; Stevenson, Roger; Schwartz, Charles; Floyd, James A B; Bentham, Jamie; Cosgrove, Catherine; Keavney, Bernard; Bhattacharya, Shoumo; Hurles, Matthew; Raymond, F Lucy.
Affiliation
  • Grozeva D; Department of Medical Genetics, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, CB2 0XY, United Kingdom.
  • Carss K; The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, United Kingdom.
  • Spasic-Boskovic O; Department of Haematology, University of Cambridge, Cambridge, CB2 0PT, United Kingdom.
  • Tejada MI; Department of Medical Genetics, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, CB2 0XY, United Kingdom.
  • Gecz J; East Anglian Medical Genetics Service, Addenbrooke's Hospital, Cambridge, CB2 0QQ, United Kingdom.
  • Shaw M; Molecular Genetics Laboratory, Genetics Service, Cruces University Hospital, BioCruces Health Research Institute, Barakaldo-Bizkaia, 48903, Spain.
  • Corbett M; Centre for Biomedical Research on Rare Diseases (CIBERER), Madrid, 28029, Spain.
  • Haan E; Department of Paediatrics and Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, 5006, Australia.
  • Thompson E; Department of Paediatrics and Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, 5006, Australia.
  • Friend K; Department of Paediatrics and Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, 5006, Australia.
  • Hussain Z; Department of Paediatrics and Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, 5006, Australia.
  • Hackett A; Department of Paediatrics and Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, 5006, Australia.
  • Field M; SA Pathology, Women's and Children's Hospital, Adelaide, South Australia, 5006, Australia.
  • Renieri A; Department of Medical Genetics, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, CB2 0XY, United Kingdom.
  • Stevenson R; Genetics of Learning Disability Service, Hunter Genetics, Waratah, New South Wales, 2298, Australia.
  • Schwartz C; Genetics of Learning Disability Service, Hunter Genetics, Waratah, New South Wales, 2298, Australia.
  • Floyd JA; Medical Genetics, University of Siena, Siena, 53100, Italy.
  • Bentham J; Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, 53100, Italy.
  • Cosgrove C; Greenwood Genetic Center, Greenwood, South Carolina, 29646.
  • Keavney B; Greenwood Genetic Center, Greenwood, South Carolina, 29646.
  • Bhattacharya S; The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, United Kingdom.
  • Hurles M; Cardiovascular Research Group, Institute of Cardiovascular Sciences, University of Manchester, Manchester, M13 9NT, United Kingdom.
  • Raymond FL; Department of Cardiovascular Medicine, University of Oxford, Wellcome Trust Centre for Human Genetics, Oxford, OX3 7BN, United Kingdom.
Hum Mutat ; 36(12): 1197-204, 2015 Dec.
Article in En | MEDLINE | ID: mdl-26350204
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genetic Association Studies / High-Throughput Nucleotide Sequencing / Intellectual Disability Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2015 Document type: Article Affiliation country: United kingdom
Fulltext
Add to My VHL
Print
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genetic Association Studies / High-Throughput Nucleotide Sequencing / Intellectual Disability Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2015 Document type: Article Affiliation country: United kingdom