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Different types of disease-causing noncoding variants revealed by genomic and gene expression analyses in families with X-linked intellectual disability.
Field, Michael J; Kumar, Raman; Hackett, Anna; Kayumi, Sayaka; Shoubridge, Cheryl A; Ewans, Lisa J; Ivancevic, Atma M; Dudding-Byth, Tracy; Carroll, Renée; Kroes, Thessa; Gardner, Alison E; Sullivan, Patricia; Ha, Thuong T; Schwartz, Charles E; Cowley, Mark J; Dinger, Marcel E; Palmer, Elizabeth E; Christie, Louise; Shaw, Marie; Roscioli, Tony; Gecz, Jozef; Corbett, Mark A.
Affiliation
  • Field MJ; NSW Genetics of Learning Disability Service, Newcastle, New South Wales, Australia.
  • Kumar R; Adelaide Medical School and Robinson Research Institute, University of Adelaide, Adelaide, South Australia, Australia.
  • Hackett A; NSW Genetics of Learning Disability Service, Newcastle, New South Wales, Australia.
  • Kayumi S; School of Biomedical Sciences and Pharmacy, University of Newcastle, Newcastle, New South Wales, Australia.
  • Shoubridge CA; Adelaide Medical School and Robinson Research Institute, University of Adelaide, Adelaide, South Australia, Australia.
  • Ewans LJ; Adelaide Medical School and Robinson Research Institute, University of Adelaide, Adelaide, South Australia, Australia.
  • Ivancevic AM; St Vincent's Clinical School, University of New South Wales, Darlinghurst, Australia.
  • Dudding-Byth T; Kinghorn Centre for Clinical Genomics, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.
  • Carroll R; Department of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, Colorado, USA.
  • Kroes T; NSW Genetics of Learning Disability Service, Newcastle, New South Wales, Australia.
  • Gardner AE; School of Biomedical Sciences and Pharmacy, University of Newcastle, Newcastle, New South Wales, Australia.
  • Sullivan P; Adelaide Medical School and Robinson Research Institute, University of Adelaide, Adelaide, South Australia, Australia.
  • Ha TT; Adelaide Medical School and Robinson Research Institute, University of Adelaide, Adelaide, South Australia, Australia.
  • Schwartz CE; Adelaide Medical School and Robinson Research Institute, University of Adelaide, Adelaide, South Australia, Australia.
  • Cowley MJ; Children's Cancer Institute, University of New South Wales, Kensington, New South Wales, Australia.
  • Dinger ME; Molecular Pathology Department, Centre for Cancer Biology, SA Pathology, Adelaide, South Australia, Australia.
  • Palmer EE; Greenwood Genetics Centre, Greenwood, South Carolina, USA.
  • Christie L; NSW Genetics of Learning Disability Service, Newcastle, New South Wales, Australia.
  • Shaw M; Kinghorn Centre for Clinical Genomics, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.
  • Roscioli T; Children's Cancer Institute, University of New South Wales, Kensington, New South Wales, Australia.
  • Gecz J; School of Biotechnology and Biomolecular Sciences, University of New South Wales, Kensington, New South Wales, Australia.
  • Corbett MA; NSW Genetics of Learning Disability Service, Newcastle, New South Wales, Australia.
Hum Mutat ; 42(7): 835-847, 2021 07.
Article in En | MEDLINE | ID: mdl-33847015
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Intellectual Disability Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2021 Type: Article Affiliation country: Australia
Fulltext
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XML
PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Intellectual Disability Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2021 Type: Article Affiliation country: Australia