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J-GLOBAL ID：201802270434248997 整理番号：18A1154964

西オーストラリア公衆衛生システムにおける未診断疾患プログラムの開始【JST・京大機械翻訳】

Initiating an undiagnosed diseases program in the Western Australian public health system

著者 (68件)：

Baynam Gareth

(Genetic Services of Western Australia, Department of Health, Government of Western Australia, Perth, Australia)

Baynam Gareth

(School of Paediatrics and Child Health, University of Western Australia, Perth, Australia)

Baynam Gareth

(Institute for Immunology and Infectious Diseases, Murdoch University, Murdoch, Australia)

Baynam Gareth

(Office of Population Health Genomics, Public Health Division, Department of Health, Government of Western Australia, Perth, Australia)

Baynam Gareth

(Telethon Kids Institute, University of Western Australia, Perth, Australia)

Baynam Gareth

(Western Australian Register of Developmental Anomalies, Perth, Australia)

Baynam Gareth

(School of Spatial Sciences, Curtin University, Perth, Australia)

Broley Stephanie

(Genetic Services of Western Australia, Department of Health, Government of Western Australia, Perth, Australia)

Bauskis Alicia

(Office of Population Health Genomics, Public Health Division, Department of Health, Government of Western Australia, Perth, Australia)

Pachter Nicholas

(Genetic Services of Western Australia, Department of Health, Government of Western Australia, Perth, Australia)

Pachter Nicholas

(School of Paediatrics and Child Health, University of Western Australia, Perth, Australia)

McKenzie Fiona

(Genetic Services of Western Australia, Department of Health, Government of Western Australia, Perth, Australia)

McKenzie Fiona

(School of Paediatrics and Child Health, University of Western Australia, Perth, Australia)

Townshend Sharron

(Genetic Services of Western Australia, Department of Health, Government of Western Australia, Perth, Australia)

Slee Jennie

(Genetic Services of Western Australia, Department of Health, Government of Western Australia, Perth, Australia)

Kiraly-Borri Cathy

(Genetic Services of Western Australia, Department of Health, Government of Western Australia, Perth, Australia)

Vasudevan Anand

(Genetic Services of Western Australia, Department of Health, Government of Western Australia, Perth, Australia)

Hawkins Anne

(Genetic Services of Western Australia, Department of Health, Government of Western Australia, Perth, Australia)

Schofield Lyn

(Genetic Services of Western Australia, Department of Health, Government of Western Australia, Perth, Australia)

Schofield Lyn

(Centre for Comparative Genomics, Murdoch University, Perth, Australia)

Helmholz Petra

(School of Spatial Sciences, Curtin University, Perth, Australia)

Helmholz Petra

(Cooperative Research Centre for Spatial Information, Perth, Australia)

Palmer Richard

(School of Spatial Sciences, Curtin University, Perth, Australia)

Palmer Richard

(Cooperative Research Centre for Spatial Information, Perth, Australia)

Kung Stefanie

(School of Spatial Sciences, Curtin University, Perth, Australia)

Kung Stefanie

(Cooperative Research Centre for Spatial Information, Perth, Australia)

Walker Caroline E.

(Office of Population Health Genomics, Public Health Division, Department of Health, Government of Western Australia, Perth, Australia)

Molster Caron

(Office of Population Health Genomics, Public Health Division, Department of Health, Government of Western Australia, Perth, Australia)

Lewis Barry

(Diagnostic Genomics, PathWest, Department of Health, Government of Western Australia, Perth, Australia)

Mina Kym

(Diagnostic Genomics, PathWest, Department of Health, Government of Western Australia, Perth, Australia)

Mina Kym

(School of Pathology and Laboratory Medicine, University of Western Australia, Perth, Australia)

Beilby John

(Diagnostic Genomics, PathWest, Department of Health, Government of Western Australia, Perth, Australia)

Beilby John

(School of Pathology and Laboratory Medicine, University of Western Australia, Perth, Australia)

Pathak Gargi

(Perth Children’s Hospital, Perth, Australia)

Poulton Cathryn

(Perth Children’s Hospital, Perth, Australia)

Groza Tudor

(Kinghorn Centre for Clinical Genomics, Garvan Institute for Medical Research, Darlinghurst, Australia)

Groza Tudor

(St. Vincent’s Clinical School, Faculty of Medicine, University of New South Wales, Darlinghurst, Australia)

Zankl Andreas

(Kinghorn Centre for Clinical Genomics, Garvan Institute for Medical Research, Darlinghurst, Australia)

Zankl Andreas

(The Children’s Hospital at Westmead, Clinical Genetics Service, Westmead, Australia)

Roscioli Tony

(Kinghorn Centre for Clinical Genomics, Garvan Institute for Medical Research, Darlinghurst, Australia)

Roscioli Tony

(St. Vincent’s Clinical School, Faculty of Medicine, University of New South Wales, Darlinghurst, Australia)

Dinger Marcel E.

(Kinghorn Centre for Clinical Genomics, Garvan Institute for Medical Research, Darlinghurst, Australia)

Mattick John S.

(Kinghorn Centre for Clinical Genomics, Garvan Institute for Medical Research, Darlinghurst, Australia)

Mattick John S.

(St. Vincent’s Clinical School, Faculty of Medicine, University of New South Wales, Darlinghurst, Australia)

Gahl William

(National Human Genome Research Institute, National Institutes of Health, Bethesda, Rockville, USA)

Gahl William

(Undiagnosed Diseases Program, Common Fund, Office of the Director, National Institutes of Health, Bethesda, Rockville, USA)

Groft Stephen

(National Centre for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland, USA)

Tifft Cynthia

(National Human Genome Research Institute, National Institutes of Health, Bethesda, Rockville, USA)

Tifft Cynthia

(Undiagnosed Diseases Program, Common Fund, Office of the Director, National Institutes of Health, Bethesda, Rockville, USA)

Taruscio Domenica

(Instituto Superiore di Sanita, National Center for Rare Diseases, Rome, Italy)

Lasko Paul

(Canadian Institutes of Health Research, Institute of Genetics, Montreal, Canada)

Kosaki Kenjiro

(Keio University School of Medicine, Tokyo, Japan)

Wilhelm Helene

(Wilhelm Foundation, Brottby, Sweden)

Melegh Bela

(Department of Medical Genetics, University of Pecs, Pecs, Hungary)

Carapetis Jonathan

(Telethon Kids Institute, University of Western Australia, Perth, Australia)

Carapetis Jonathan

(Perth Children’s Hospital, Perth, Australia)

Jana Sayanta

(King Edward Memorial Hospital, Perth, Australia)

Chaney Gervase

(Perth Children’s Hospital, Perth, Australia)

Johns Allison

(King Edward Memorial Hospital, Perth, Australia)

Owen Peter Wynn

(King Edward Memorial Hospital, Perth, Australia)

Daly Frank

(Perth Children’s Hospital, Perth, Australia)

Weeramanthri Tarun

(Public Health Division, Department of Health, Government of Western Australia, Perth, Australia)

Dawkins Hugh

(Office of Population Health Genomics, Public Health Division, Department of Health, Government of Western Australia, Perth, Australia)

Dawkins Hugh

(Centre for Population Health Research, Curtin Health Innovation Research Institute, Curtin University of Technology, Perth, Australia)

Dawkins Hugh

(School of Pathology and Laboratory Medicine, University of Western Australia, Perth, Australia)

Dawkins Hugh

(Centre for Comparative Genomics, Murdoch University, Perth, Australia)

Goldblatt Jack

(Genetic Services of Western Australia, Department of Health, Government of Western Australia, Perth, Australia)

Goldblatt Jack

(School of Paediatrics and Child Health, University of Western Australia, Perth, Australia)

資料名：

Orphanet Journal of Rare Diseases (Web) (Orphanet Journal of Rare Diseases (Web))

巻： 12 号： 1 ページ： 83 発行年： 2017年
JST資料番号： U7532A ISSN： 1750-1172 資料種別：逐次刊行物 (A)
記事区分：原著論文発行国：イギリス (GBR) 言語：英語 (EN)

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