Mutational spectrum of cystic fibrosis in the Lebanese population.

[1]  C. Acerini,et al.  Cystic fibrosis related diabetes mellitus - diagnostic and management challenges. , 2010, Current diabetes reviews.

[2]  Olafur Baldursson,et al.  [Cystic fibrosis--review]. , 2008, Laeknabladid.

[3]  C. Farra,et al.  Cystic fibrosis: a new mutation in the Lebanese population. , 2008, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

[4]  X. Estivill,et al.  Spectrum of Mutations in the CFTR Gene in Cystic Fibrosis Patients of Spanish Ancestry , 2007, Annals of human genetics.

[5]  J. Draaisma,et al.  Investigation for cystic fibrosis in infants with jejunoileal atresia in the Netherlands: a 35-year experience with 114 cases , 2007, European Journal of Pediatrics.

[6]  G. Feldman,et al.  Cystic Fibrosis testing among Arab-Americans , 2006, Genetics in Medicine.

[7]  I. Lerer,et al.  Mutation spectrum in Jewish cystic fibrosis patients in Israel: Implication to carrier screening , 2005, American journal of medical genetics. Part A.

[8]  O. Fernandes,et al.  Molecular Analysis of 23 Exons of the CFTR Gene in Brazilian Patients Leads to the Finding of Rare Cystic Fibrosis Mutations , 2005, Human biology.

[9]  C. Scriver,et al.  The Metabolic and Molecular Bases of Inherited Disease, 8th Edition 2001 , 2001, Journal of Inherited Metabolic Disease.

[10]  M. Tzetis,et al.  Cystic fibrosis in Greece: molecular diagnosis, haplotypes, prenatal diagnosis and carrier identification amongst high‐risk individuals , 2003, Clinical genetics.

[11]  H. Eskandarani.  Cystic fibrosis transmembrane regulator gene mutations in Bahrain. , 2002, Journal of tropical pediatrics.

[12]  M. Kambouris,et al.  Cystic fibrosis in a child from Syria , 2002, Annals of tropical paediatrics.

[13]  M. Kambouris,et al.  Heterogeneity of the cystic fibrosis phenotype in a large kindred family in Qatar with cystic fibrosis mutation (I1234V). , 2001, Journal of tropical pediatrics.

[14]  H. Manal,et al.  Cystic fibrosis in Arabs: a prototype from Jordan , 2000, Annals of tropical paediatrics.

[15]  B. Meyer,et al.  Identification of novel mutations in Arabs with cystic fibrosis and their impact on the cystic fibrosis transmembrane regulator mutation detection rate in Arab populations , 2000, European Journal of Pediatrics.

[16]  L. Strmečki,et al.  Mutational analysis of 30 Slovenian cystic fibrosis patients compared to known Slovenian and European CF mutation spectra , 2000, Pflügers Archiv.

[17]  I. Lerer,et al.  Cystic fibrosis mutations in Israeli Arab patients , 1999, Human mutation.

[18]  E. Girodon,et al.  Determination of the prevalence of cystic fibrosis in the United Arab Emirates by genetic carrier screening , 1999, Clinical genetics.

[19]  H. Banjar.  Geographic distribution of cystic fibrosis transmembrane regulator gene mutations in Saudi Arabia. , 1999, Eastern Mediterranean health journal = La revue de sante de la Mediterranee orientale = al-Majallah al-sihhiyah li-sharq al-mutawassit.

[20]  G. Cutting,et al.  The diagnosis of cystic fibrosis: a consensus statement. Cystic Fibrosis Foundation Consensus Panel. , 1998, The Journal of pediatrics.

[21]  A. Hamosh,et al.  Comparison of the clinical manifestations of cystic fibrosis in black and white patients. , 1998, The Journal of pediatrics.

[22]  T. Dörk,et al.  Novel and characteristic CFTR mutations in Saudi Arab children with severe cystic fibrosis. , 1997, Journal of medical genetics.

[23]  A. Mégarbané,et al.  Cystic fibrosis in Lebanon: distribution of CFTR mutations among Arab communities , 1997, Human Genetics.

[24]  X. Estivill,et al.  Geographic distribution and regional origin of 272 cystic fibrosis mutations in European populations , 1997 .

[25]  B. Kerem,et al.  Two novel mutations in the CFTR gene: W1089X in exon 17B and 4010delTATT in exon 21. , 1994, Human molecular genetics.

[26]  B. Kerem,et al.  Correlation between genotype and phenotype in patients with cystic fibrosis. , 1994, The New England journal of medicine.

[27]  J. Cheadle,et al.  Population variation of common cystic fibrosis mutations , 1994 .

[28]  D. Glavač,et al.  Identification of a rare cystic fibrosis mutation (S4X) in a Slovenian population. , 1993, Human molecular genetics.

[29]  C. Boeck.  Correlation between genotype and phenotype in patients with cystic fibrosis , 1993 .