A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases

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作者： Kingsmore, Stephen F. ^[1] ; Smith, Laurie D. ^[2] ; Kunard, Chris M. ^[3] ; Bainbridge, Matthew ^[4] ; Batalov, Sergey ^[5] ; Benson, Wendy ^[6] ; Blincow, Eric ^[7] ; Caylor, Sara ^[8] ; Chambers, Christina ^[9] ; Del Angel, Guillermo ; Dimmock, David P. ; Ding, Yan ; Ellsworth, Katarzyna ; Feigenbaum, Annette ; Frise, Erwin ; Green, Robert C. ; Guidugli, Lucia ; Hall, Kevin P. ; Hansen, Christian ; Hobbs, Charlotte A. ; Kahn, Scott D. ; Kiel, Mark ; Van Der Kraan, Lucita ; Krilow, Chad ; Kwon, Yong H. ; Madhavrao, Lakshminarasimha ; Le, Jennie ; Lefebvre, Sebastien ; Mardach, Rebecca ; Mowrey, William R. ; Oh, Danny ; Owen, Mallory J. ; Powley, George ; Scharer, Gunter ; Shelnutt, Seth ; Tokita, Mari ; Mehtalia, Shyamal S. ; Oriol, Albert ; Papadopoulos, Stavros ; Perry, James ; Rosales, Edwin ; Sanford, Erica ; Schwartz, Steve ; Tran, Duke ; Reese, Martin G. ; Wright, Meredith ; Veeraraghavan, Narayanan ; Wigby, Kristen ; Willis, Mary J. ; Wolen, Aaron R. ; Defay, Thomas

作者单位： Rady Childrens Inst Genom Med ^[1] Illumina Inc ^[2] Dept Pediat,Univ Calif San Diego ^[3] Astra Zeneca Rare Dis,Alexion ^[4] Fabr Genom Inc ^[5] Ariadne Labs,Mass Gen Brigham Broad Inst ^[6] Genomenon Inc ^[7] TileDB Inc ^[8] Rady Childrens Hospital San Diego,Rady Childrens Hosp ^[9]

关键词 ILL INFANTS DISORDERS UTILITY MANAGEMENT HEALTH LIST

发布时间 2023-05-21

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The American Journal of Human Genetics

2022年109卷9期

1605-1619页

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A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases

The American Journal of Human Genetics

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The American Journal of Human Genetics

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A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases

The American Journal of Human Genetics

相似文献

The American Journal of Human Genetics

相关期刊

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