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Barriers and Considerations for Diagnosing Rare Diseases in Indigenous Populations.
D'Angelo, Carla S; Hermes, Azure; McMaster, Christopher R; Prichep, Elissa; Richer, Étienne; van der Westhuizen, Francois H; Repetto, Gabriela M; Mengchun, Gong; Malherbe, Helen; Reichardt, Juergen K V; Arbour, Laura; Hudson, Maui; du Plessis, Kelly; Haendel, Melissa; Wilcox, Phillip; Lynch, Sally Ann; Rind, Shamir; Easteal, Simon; Estivill, Xavier; Thomas, Yarlalu; Baynam, Gareth.
Afiliación
  • D'Angelo CS; IRDiRC Scientific Secretariat, National Institute for Health and Medical Research, Paris, France.
  • Hermes A; National Centre for Indigenous Genomics, Australian National University, Canberra, ACT, Australia.
  • McMaster CR; Department of Pharmacology, Dalhousie University, Halifax, NS, Canada.
  • Prichep E; Precision Medicine, Platform on Shaping the Future of Health and Healthcare, World Economic Forum, San Francisco, CA, United States.
  • Richer É; Institute of Genetics, Canadian Institutes of Health Research, Government of Canada, Ottawa, ON, Canada.
  • van der Westhuizen FH; Human Metabolomics, North-West University, Potchefstroom, South Africa.
  • Repetto GM; Facultad de Medicina, Center for Genetics and Genomics, Clinica Alemana Universidad del Desarrollo, Santiago, Chile.
  • Mengchun G; Institute of Health Management, Southern Medical University, Guangdong, China.
  • Malherbe H; KwaZulu-Natal Research Innovation and Sequencing Platform, University of KwaZulu-Natal, Durban, South Africa.
  • Reichardt JKV; Rare Diseases South Africa, Johannesburg, South Africa.
  • Arbour L; Australian Institute of Tropical Health and Medicine, James Cook University, Smithfield, QLD, Australia.
  • Hudson M; Department of Medical Genetics, University of British Columbia, Victoria, BC, Canada.
  • du Plessis K; Faculty of Maori and Indigenous Studies, University of Waikato, Hamilton, New Zealand.
  • Haendel M; Rare Diseases South Africa, Johannesburg, South Africa.
  • Wilcox P; Oregon Clinical and Translational Research Institute, Oregon Health and Science University, Portland, OR, United States.
  • Lynch SA; Department of Mathematics and Statistics, University of Otago, Dunedin, New Zealand.
  • Rind S; National Rare Disease Office, Mater Misericordiae University Hospital, Dublin, Ireland.
  • Easteal S; Academic Centre on Rare Diseases, University College Dublin, Dublin, Ireland.
  • Estivill X; Western Australian Register of Developmental Anomalies, Perth, WA, Australia.
  • Thomas Y; National Centre for Indigenous Genomics, Australian National University, Canberra, ACT, Australia.
  • Baynam G; Quantitative Genomics Laboratories (qgenomics), Esplugues de Llobregat, Barcelona, Spain.
Front Pediatr ; 8: 579924, 2020.
Article en En | MEDLINE | ID: mdl-33381478
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Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Guideline Idioma: En Año: 2020 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Guideline Idioma: En Año: 2020 Tipo del documento: Article