Cystic fibrosis: A new mutation in the Lebanese population
Author:
Publisher
Elsevier BV
Subject
Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health
Reference20 articles.
1. Cystic fibrosis: a worldwide analysis of CFTR mutations–correlation with incidence data and application to screening;Bobadilla;Hum Mutat,2002
2. The geographic distribution of cystic fibrosis mutations gives clues about population origins;Dawson;Eur J Pediatr,2000
3. Complete map of cystic fibrosis mutation DF508 frequencies in Western Europe and correlation between mutation frequencies and incidence of disease;Lucotte;Hum Biol,1995
4. Cystic fibrosis in Lebanon: distribution of CFTR mutations among Arab communities;Desgeorges;Hum Genet,1997
5. Two novel mutations in the CFTR gene: W1089X in exon 17B and 4010delTATT in exon 21;Shoshani;Hum Mol Genet,1994
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1. CFTR mutational screening by next‐generation sequencing reveals novel variants and a high carrier rate in a Middle Eastern population;Annals of Human Genetics;2021-12-09
2. Spectrum of mutations of cystic fibrosis in the 22 Arab countries: A systematic review;Respirology;2018-11-12
3. Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene mutations in North Egyptian population: implications for the genetic diagnosis in Egypt;Cellular and Molecular Biology;2016-11-30
4. Respiratory disorders in the Middle East: A review;Respirology;2011-06-28
5. Mutational spectrum of cystic fibrosis in the Lebanese population;Journal of Cystic Fibrosis;2010-12
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