Your browser doesn't support javascript.
loading
Characterising heart rhythm abnormalities associated with Xp22.31 deletion.
Wren, Georgina; Baker, Emily; Underwood, Jack; Humby, Trevor; Thompson, Andrew; Kirov, George; Escott-Price, Valentina; Davies, William.
Afiliação
  • Wren G; School of Psychology, Cardiff University, Cardiff, UK.
  • Baker E; Dementia Research Institute, Cardiff University, Cardiff, UK.
  • Underwood J; MRC Centre for Neuropsychiatric Genetics and Genomics and Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK.
  • Humby T; MRC Centre for Neuropsychiatric Genetics and Genomics and Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK.
  • Thompson A; Neuroscience and Mental Health Innovation Institute, Cardiff University, Cardiff, UK.
  • Kirov G; School of Psychology, Cardiff University, Cardiff, UK.
  • Escott-Price V; MRC Centre for Neuropsychiatric Genetics and Genomics and Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK.
  • Davies W; Neuroscience and Mental Health Innovation Institute, Cardiff University, Cardiff, UK.
J Med Genet ; 60(7): 636-643, 2023 07.
Article em En | MEDLINE | ID: mdl-36379544
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ictiose Ligada ao Cromossomo X / Cardiopatias Congênitas Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: J Med Genet Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Reino Unido
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ictiose Ligada ao Cromossomo X / Cardiopatias Congênitas Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: J Med Genet Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Reino Unido