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Title
Precision newborn screening for lysosomal disorders
Authors
Keywords
-
Journal
GENETICS IN MEDICINE
Volume -, Issue -, Pages -
Publisher
Springer Nature
Online
2017-11-10
DOI
10.1038/gim.2017.194
References
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Related references
Note: Only part of the references are listed.- Newborn screening for six lysosomal storage disorders in a cohort of Mexican patients: Three-year findings from a screening program in a closed Mexican health system
- (2017) Juana Inés Navarrete-Martínez et al. MOLECULAR GENETICS AND METABOLISM
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- Measurement of psychosine in dried blood spots — a possible improvement to newborn screening programs for Krabbe disease
- (2015) Coleman T. Turgeon et al. JOURNAL OF INHERITED METABOLIC DISEASE
- Lysosomal Storage Disorder Screening Implementation: Findings from the First Six Months of Full Population Pilot Testing in Missouri
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- Improved Reagents for Newborn Screening of Mucopolysaccharidosis Types I, II, and VI by Tandem Mass Spectrometry
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- Fifty years of newborn screening
- (2014) R. Rodney Howell MOLECULAR GENETICS AND METABOLISM
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- Siblings With Mitochondrial Acetoacetyl-CoA Thiolase Deficiency Not Identified by Newborn Screening
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- Informatics Infrastructure for Syndrome Surveillance, Decision Support, Reporting, and Modeling of Critical Illness
- (2010) Vitaly Herasevich et al. MAYO CLINIC PROCEEDINGS
- False Positive Newborn Screening Results Are Not Always Benign
- (2010) D.R. Morrison et al. Public Health Genomics
- Pompe's disease
- (2008) Ans T van der Ploeg et al. LANCET
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