A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases
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Published:2022-09
Issue:9
Volume:109
Page:1605-1619
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ISSN:0002-9297
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Container-title:The American Journal of Human Genetics
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language:en
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Short-container-title:The American Journal of Human Genetics
Author:
Kingsmore Stephen F.ORCID, Smith Laurie D., Kunard Chris M., Bainbridge Matthew, Batalov Sergey, Benson Wendy, Blincow Eric, Caylor Sara, Chambers Christina, 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
Subject
Genetics (clinical),Genetics
Reference72 articles.
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