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Undiagnosed Diseases Network International (UDNI): White paper for global actions to meet patient needs.
Taruscio, Domenica; Groft, Stephen C; Cederroth, Helene; Melegh, Béla; Lasko, Paul; Kosaki, Kenjiro; Baynam, Gareth; McCray, Alexa; Gahl, William A.
Afiliação
  • Taruscio D; National Center for Rare Diseases, Istituto Superiore di Sanità, Rome, Italy. Electronic address: domenica.taruscio@iss.it.
  • Groft SC; National Center for Advancing Translational Sciences, National Institutes of Health, United States.
  • Cederroth H; Wilhelm Foundation, Sweden.
  • Melegh B; Department of Medical Genetics, University of Pécs, Hungary.
  • Lasko P; Department of Biology, McGill University, Montreal, Canada.
  • Kosaki K; Center for Medical Genetics, Keio University School of Medicine, Tokyo, Japan.
  • Baynam G; Princess Margaret and King Edward Memorial Hospitals, Perth, Australia; Office of Population Health, Public Health Division, WA Department of Health, Australia; Telethon Kids Institute, Perth, Australia; Western Australian Registry of Developmental Anomalies, Perth, Australia; School of Paediatrics
  • McCray A; Center for Biomedical Informatics, Department of Medicine, Harvard Medical School, Boston, Massachusetts, United States.
  • Gahl WA; NIH Undiagnosed Diseases Program, National Human Genome Research Institute, National Institutes of Health, United States.
Mol Genet Metab ; 116(4): 223-5, 2015 Dec.
Article em En | MEDLINE | ID: mdl-26596705
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 11_ODS3_cobertura_universal / 2_ODS3 Base de dados: MEDLINE Assunto principal: Saúde Global / Doenças Raras / Programas Governamentais Tipo de estudo: Guideline / Prognostic_studies Limite: Humans País/Região como assunto: America do norte Idioma: En Revista: Mol Genet Metab Ano de publicação: 2015 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 11_ODS3_cobertura_universal / 2_ODS3 Base de dados: MEDLINE Assunto principal: Saúde Global / Doenças Raras / Programas Governamentais Tipo de estudo: Guideline / Prognostic_studies Limite: Humans País/Região como assunto: America do norte Idioma: En Revista: Mol Genet Metab Ano de publicação: 2015 Tipo de documento: Article