Utility of a very high IRT/No mutation referral category in cystic fibrosis newborn screening-Reference-Cited by-同舟云学术

Utility of a very high IRT/No mutation referral category in cystic fibrosis newborn screening

Published:2015-06-22 Issue:8 Volume:50 Page:771-780
ISSN:8755-6863
Container-title:Pediatric Pulmonology
language:en
Short-container-title:Pediatr Pulmonol.

Author:

Kay Denise M.¹,Langfelder-Schwind Elinor²,DeCelie-Germana Joan³,Sharp Jack K.⁴,Maloney Breanne¹,Tavakoli Norma P.¹⁵,Saavedra-Matiz Carlos A.¹,Krein Lea M.¹,Caggana Michele¹,Kier Catherine⁶,

Affiliation:

1. Division of Genetics; Wadsworth Center; New York State Department of Health; Albany New York

2. The Cystic Fibrosis Center; Mount Sinai Beth Israel; New York New York

3. Cohen Children's Medical Center of New York; Great Neck New York

4. Departments of Pediatrics; Duke University, Durham; NC and State University of New York (SUNY) at Buffalo; Buffalo New York

5. Department of Biomedical Sciences; University at Albany; Albany New York

6. University Medical Center at Stony Brook; Stony Brook New York

Funder

Wadsworth Center, New York State Department of Health

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology, and Child Health

Reference31 articles.

1. Immunoreactive trypsinogen (IRT) as a biomarker for cystic fibrosis: challenges in newborn dried blood spot screening;Therrell;Mol Genet Metab,2012

2. Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus report;Farrell;J Pediatr,2008

3. Laboratory standards and guidelines for population-based cystic fibrosis carrier screening;Grody;Genet Med,2001

4. Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel;Watson;Genet Med,2004

5. Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice;Castellani;J Cyst Fibros,2008

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