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Patrick Hopkins, C. Campbell, Tracy Klug, Sharmini Rogers, Julie Raburn-Miller, Jami Kiesling (2015)
Lysosomal storage disorder screening implementation: findings from the first six months of full population pilot testing in Missouri.The Journal of pediatrics, 166 1
D. Matern, D. Gavrilov, D. Oglesbee, K. Raymond, P. Rinaldo, S. Tortorelli (2015)
Newborn screening for lysosomal storage disorders.Seminars in perinatology, 39 3
R. Sista, Tong Wang, Ning Wu, C. Graham, A. Eckhardt, T. Winger, V. Srinivasan, D. Bali, D. Millington, V. Pamula (2013)
Multiplex newborn screening for Pompe, Fabry, Hunter, Gaucher, and Hurler diseases using a digital microfluidic platform.Clinica chimica acta; international journal of clinical chemistry, 424
B. Burton, J. Charrow, G. Hoganson, D. Waggoner, B. Tinkle, S. Braddock, Michael Schneider, D. Grange, C. Nash, Heather Shryock, Rebecca Barnett, Rong Shao, K. Basheeruddin, G. Dizikes (2017)
Newborn Screening for Lysosomal Storage Disorders in Illinois: The Initial 15‐Month ExperienceThe Journal of Pediatrics, 190
This study describes the incidence rates for 4 lysosomal storage disorders from 4 years of full-population testing of all newborns in Missouri.
JAMA Pediatrics – American Medical Association
Published: Jul 29, 2018
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