New York State Cystic Fibrosis Consortium: The First 2.5 Years of Experience With Cystic Fibrosis Newborn Screening in an Ethnically Diverse Population
Author:
Affiliation:
1. Departments of Pediatrics
2. Obstetrics and Gynecology, Long Island College Hospital, Brooklyn, New York
3. Division of Medical Genetics, Department of Pediatrics, Beth Israel Medical Center, New York, New York
Abstract
Publisher
American Academy of Pediatrics (AAP)
Subject
Pediatrics, Perinatology and Child Health
Link
https://publications.aap.org/pediatrics/article-pdf/119/2/e460/1118173/zpe0020700e460.pdf
Reference32 articles.
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2. Cystic Fibrosis Genetic Analysis Consortium. Cystic fibrosis mutation database. Updated July 26, 2006. Available at: www.genet.sickkids.on.ca/cftr/app. Accessed August 22, 2006
3. Richards CS, Bardley LA, Amos J, et al. Technical standards and guidelines for CFTR mutation testing. Genet Med. 2002;4:379–391
4. Farrell PM, Kosorok MR, Rock MJ, Laxova A, Zeng L, Lai HC. Early diagnosis of cystic fibrosis through neonatal screening prevents severe malnutrition and improves long-term growth. Wisconsin Cystic Fibrosis Neonatal Screening Study Group. Pediatrics. 2001;107:1–13
5. Wilfond BS, Gollust SE. Policy issues for expanding newborn screening programs: the cystic fibrosis newborn screening experience in the United States. J Pediatr. 2005;146:668–674
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