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Contribution of de novo and inherited rare CNVs to very preterm birth.
Wong, Hilary S; Wadon, Megan; Evans, Alexandra; Kirov, George; Modi, Neena; O'Donovan, Michael C; Thapar, Anita.
Affiliation
  • Wong HS; Department of Paediatrics, Cambridge University, Cambridge, UK.
  • Wadon M; MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, UK.
  • Evans A; MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, UK.
  • Kirov G; MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, UK.
  • Modi N; Section of Neonatal Medicine, Imperial College London, London, UK.
  • O'Donovan MC; MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, UK.
  • Thapar A; MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, UK thapar@cardiff.ac.uk.
J Med Genet ; 57(8): 552-557, 2020 08.
Article in En | MEDLINE | ID: mdl-32051258
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genetic Predisposition to Disease / Premature Birth / Genome-Wide Association Study / DNA Copy Number Variations Type of study: Guideline / Prognostic_studies Limits: Female / Humans / Male / Newborn / Pregnancy Language: En Journal: J Med Genet Year: 2020 Document type: Article Affiliation country: Reino Unido
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genetic Predisposition to Disease / Premature Birth / Genome-Wide Association Study / DNA Copy Number Variations Type of study: Guideline / Prognostic_studies Limits: Female / Humans / Male / Newborn / Pregnancy Language: En Journal: J Med Genet Year: 2020 Document type: Article Affiliation country: Reino Unido