Technological Journey From Colorimetric to Tandem Mass Spectrometric Measurements in the Diagnostic Investigation for Phenylketonuria-Reference-Cited by-同舟云学术

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Technological Journey From Colorimetric to Tandem Mass Spectrometric Measurements in the Diagnostic Investigation for Phenylketonuria

Published:2016-07-29 Issue: Volume:4 Page:232640981667173
ISSN:2326-4098
Container-title:Journal of Inborn Errors of Metabolism and Screening
language:en
Short-container-title:Journal of Inborn Errors of Metabolism and Screening

Author:

Chace Donald H.¹,Hannon William H.²

Affiliation:

1. Pediatrix Analytical, Mednax Centers for Research, Education and Quality, Sunrise, FL, USA

2. CDC Foundation and Newborn Screening Branch, Centers for Disease Control and Prevention (CDC), Atlanta, GA, USA

Publisher

FapUNIFESP (SciELO)

Subject

Genetics (clinical),Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health

Link

http://journals.sagepub.com/doi/pdf/10.1177/2326409816671733

Reference44 articles.

1. The Discovery of Phenylketonuria: The Story of a Young Couple, Two Retarded Children, and a Scientist

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Over 50 Years of Population‐Based Dried Blood Spot Sampling of Newborns; Assuring Quality Testing and Lessons Learned;Patient Centric Blood Sampling and Quantitative Bioanalysis;2023-10-13

2. Birth prevalence of phenylalanine hydroxylase deficiency: a systematic literature review and meta-analysis;Orphanet Journal of Rare Diseases;2021-06-03

3. Metabolic screening and metabolomics analysis in the Intellectual Developmental Disorders Mexico Study;Salud Pública de México;2017-07-25

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