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Incidence of Fragile X syndrome in Ireland.
O'Byrne, James J; Sweeney, Michael; Donnelly, Deirdre E; Lambert, Deborah M; Beattie, Eleanor D; Gervin, Celine M; Barton, David E; Lynch, Sally A.
Afiliação
  • O'Byrne JJ; Department of Clinical Genetics, Our Lady's Children's Hospital Crumlin, Crumlin, Dublin, Ireland.
  • Sweeney M; Department of Clinical Genetics, Our Lady's Children's Hospital Crumlin, Crumlin, Dublin, Ireland.
  • Donnelly DE; Northern Ireland Regional Genetics Centre, Belfast Health and Social Care Trust/City Hospital, Belfast, Northern Ireland.
  • Lambert DM; National Rare Diseases Office, Mater Misericordiae Hospital, Dublin, Ireland.
  • Beattie ED; Northern Ireland Regional Genetics Centre, Belfast Health and Social Care Trust/City Hospital, Belfast, Northern Ireland.
  • Gervin CM; Northern Ireland Regional Genetics Centre, Belfast Health and Social Care Trust/City Hospital, Belfast, Northern Ireland.
  • Barton DE; Department of Clinical Genetics and University College Dublin School of Medicine and Medical Sciences, Our Lady's Children's Hospital Crumlin, Crumlin, Dublin, Ireland.
  • Lynch SA; National Rare Diseases Office, Mater Misericordiae Hospital, Dublin, Ireland.
Am J Med Genet A ; 173(3): 678-683, 2017 Mar.
Article em En | MEDLINE | ID: mdl-28157260
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Síndrome do Cromossomo X Frágil Tipo de estudo: Diagnostic_studies / Incidence_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male País/Região como assunto: Europa Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Irlanda
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Síndrome do Cromossomo X Frágil Tipo de estudo: Diagnostic_studies / Incidence_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male País/Região como assunto: Europa Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Irlanda