Your browser doesn't support javascript.
loading
Advancing diagnosis and research for rare genetic diseases in Indigenous peoples.
Baynam, Gareth; Julkowska, Daria; Bowdin, Sarah; Hermes, Azure; McMaster, Christopher R; Prichep, Elissa; Richer, Étienne; van der Westhuizen, Francois H; Repetto, Gabriela M; 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; Caron, Nadine; Chongo, Meck; Thomas, Yarlalu; Letinturier, Mary Catherine V; Vorster, Barend Christiaan.
Afiliação
  • Baynam G; Rare Care Centre and Genetic Services of Western Australia, Department of Health, Government of Western Australia, Perth, Western Australia, Australia. gareth.baynam@health.wa.gov.au.
  • Julkowska D; Faculty of Health and Medicine, Division of Pediatrics, University of Western Australia, Perth, Western Australia, Australia. gareth.baynam@health.wa.gov.au.
  • Bowdin S; Telethon Kids Institute, University of Western Australia, Perth, Western Australia, Australia. gareth.baynam@health.wa.gov.au.
  • Hermes A; Faculty of Medicine, University of Notre Dame, Fremantle, Western Australia, Australia. gareth.baynam@health.wa.gov.au.
  • McMaster CR; Faculty of Science and Engineering, Spatial Sciences, Curtin University, Perth, Western Australia, Australia. gareth.baynam@health.wa.gov.au.
  • Prichep E; Faculty of Medicine, Notre Dame University, Perth, Western Australia, Australia. gareth.baynam@health.wa.gov.au.
  • Richer É; School of Population and Global Health, University of Melbourne, Melbourne, Victoria, Australia. gareth.baynam@health.wa.gov.au.
  • van der Westhuizen FH; IRDiRC Scientific Secretariat, French National Institute of Health and Medical Research (Inserm), Paris, France.
  • Repetto GM; Department of Clinical Genetics, Addenbrooke's Hospital, Cambridge, UK.
  • Malherbe H; National Centre for Indigenous Genomics, Australian National University, Canberra, Australian Capital Territory, Australia.
  • Reichardt JKV; Department of Pharmacology, Dalhousie University, Halifax, Nova Scotia, Canada.
  • Arbour L; Institute of Genetics, Canadian Institutes of Health Research, Halifax, Nova Scotia, Canada.
  • Hudson M; Platform on Shaping the Future of Health and Healthcare, World Economic Forum, New York, NY, USA.
  • du Plessis K; Institute of Genetics, Canadian Institutes of Health Research, Halifax, Nova Scotia, Canada.
  • Haendel M; Human Metabolomics, North-West University, Potchefstroom, South Africa.
  • Wilcox P; Facultad de Medicina, Center for Genetics and Genomics, Clinica Alemana Universidad del Desarrollo, Santiago, Chile.
  • Lynch SA; Department of Biochemistry, Genetics and Microbiology, University of Pretoria, Pretoria, South Africa.
  • Rind S; Rare Diseases South Africa, Johannesburg, South Africa.
  • Easteal S; Australian Institute of Tropical Health and Medicine, James Cook University, Smithfield, Queensland, Australia.
  • Estivill X; Department of Medical Genetics, University of British Columbia, Victoria, British Columbia, Canada.
  • Caron N; Faculty of Maori and Indigenous Studies, University of Waikato, Hamilton, New Zealand.
  • Chongo M; Rare Diseases South Africa, Johannesburg, South Africa.
  • Thomas Y; Oregon Clinical and Translational Research Institute, Oregon Health and Science University, Portland, OR, USA.
  • Letinturier MCV; Department of Mathematics and Statistics, University of Otago, Dunedin, New Zealand.
  • Vorster BC; National Rare Disease Office, Mater Misericordiae University Hospital, Dublin, Ireland.
Nat Genet ; 56(2): 189-193, 2024 Feb.
Article em En | MEDLINE | ID: mdl-38332370
Assuntos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Raras / Povos Indígenas Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Nat Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Austrália
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Raras / Povos Indígenas Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Nat Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Austrália