The contribution of X-linked coding variation to severe developmental disorders.
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| Title: | The contribution of X-linked coding variation to severe developmental disorders. |
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| Authors: | Martin HC; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK. hcm@sanger.ac.uk., Gardner EJ; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK., Samocha KE; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK., Kaplanis J; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK., Akawi N; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.; Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK., Sifrim A; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.; Department of Human Genetics, University of Leuven, Leuven, Belgium., Eberhardt RY; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK., Tavares ALT; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.; Department of Clinical Genetics, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.; Genomics England, Queen Mary University of London, London, EC1M 6BQ, UK., Neville MDC; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK., Niemi MEK; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.; Institute for Molecular Medicine Finland, University of Helsinki, Tukholmankatu 8, Helsinki, FI-00014, Finland., Gallone G; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.; Max Planck Institute for Molecular Genetics, Ihnestraße 63, 14195, Berlin, Germany., McRae J; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.; Illumina Inc., 5200 Illumina Way, San Diego, CA, 92122, USA., Wright CF; Institute of Biomedical & Clinical Science, University of Exeter Medical School, Exeter, EX2 5DW, UK., FitzPatrick DR; MRC Human Genetics Unit, MRC IGMM, University of Edinburgh, Western General Hospital, Edinburgh, EH4 2XU, UK., Firth HV; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.; Department of Clinical Genetics, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK., Hurles ME; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK. |
| Corporate Authors: | Deciphering Developmental Disorders Study |
| Source: | Nature communications [Nat Commun] 2021 Jan 27; Vol. 12 (1), pp. 627. Date of Electronic Publication: 2021 Jan 27. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| ISSN: | 2041-1723 |
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| DOI: | 10.1038/s41467-020-20852-3 |
