The impact of a national population carrier screening program on cystic fibrosis birth rate and age at diagnosis: Implications for newborn screening

Author:

Stafler Patrick,Mei-Zahav Meir,Wilschanski Michael,Mussaffi Huda,Efrati Ori,Lavie Moran,Shoseyov David,Cohen-Cymberknoh Malena,Gur Michal,Bentur Lea,Livnat Galit,Aviram Micha,Alkrinawi Soliman,Picard Elie,Prais Dario,Steuer Guy,Inbar Ori,Kerem Eitan,Blau Hannah

Publisher

Elsevier BV

Subject

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

Reference34 articles.

1. Guidelines for diagnosis of cystic fibrosis in newborns through older adults: cystic fibrosis foundation consensus report;Farrell;J Pediatr,2008

2. Highly variable incidence of cystic fibrosis and different mutation distribution among different Jewish ethnic groups in Israel;Kerem;Hum Genet,1995

3. Screening for five mutations detects 97% of cystic fibrosis (CF) chromosomes and predicts a carrier frequency of 1:29 in the Jewish Ashkenazi population;Abeliovich;Am J Hum Genet,1992

4. Cystic fibrosis mutations in Israeli Arab patients;Laufer-Cahana;Hum Mutat,1999

5. 486: Update on carrier screening for cystic fibrosis;Committee Opinion;Obstet Gynecol,2011

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