A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases
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Laurie D. Smith | Scott D. Kahn | G. Del Angel | S. Kingsmore | K. Hall | E. Frise | M. G. Reese | Du Tran | M. Bainbridge | Serge Batalov | Jennie M. Le | N. Veeraraghavan | Wendy Benson | D. Dimmock | Kristen Wigby | Yan Ding | Katarzyna A Ellsworth | E. Sanford | M. Tokita | Thomas Defay | A. Wolen | A. Feigenbaum | W. Mowrey | Stavros Papadopoulos | G. Scharer | L. Guidugli | R. C. Green | Mark W. Kiel | R. Mardach | Sara A. Caylor | Christian Hansen | Chad Krilow | S. Lefebvre | C. Hobbs | L. Madhavrao | Christina Chambers | M. Owen | J. Le | S. Batalov | Chris M Kunard | Shyamal S Mehtalia | Y. Kwon | James Perry | Albert Oriol | Eric Blincow | Lucita Van Der Kraan | Danny Oh | G. Powley | Seth Shelnutt | Edwin Rosales | Steve Schwartz | M. Wright | M. J. Willis | Mallory J. Owen | Charlotte A. Hobbs | K. Wigby | Chris M. Kunard | Shyamal S. Mehtalia | Charlotte A Hobbs | Duke Tran | L. Van Der Kraan