Related references
Note: Only part of the references are listed.The Effect of CFTR Modulators on Airway Infection in Cystic Fibrosis
Caitlyn Harvey et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2022)
Cystic fibrosis in low and middle-income countries (LMIC): A view from four different regions of the world
Luiz Vicente Ribeiro Ferreira da Silva Filho et al.
PAEDIATRIC RESPIRATORY REVIEWS (2021)
Analysis of rearrangements of the CFTR gene in patients from Turkey with CFTR-related disorders: frequent exon 2 deletion
Mehmet Bugrahan Duz et al.
JOURNAL OF HUMAN GENETICS (2021)
Genotype patterns for mutations of the cystic fibrosis transmembrane conductance regulator gene: a retrospective descriptive study from Saudi Arabia
Hanaa Hasan Banjar et al.
ANNALS OF SAUDI MEDICINE (2020)
Cystic fibrosis carriers are at increased risk for a wide range of cystic fibrosis-related conditions
Aaron C. Miller et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2020)
CFTR Modulators: The Changing Face of Cystic Fibrosis in the Era of Precision Medicine
Miqueias Lopes-Pacheco
FRONTIERS IN PHARMACOLOGY (2020)
Analysis of CFTR Mutation Spectrum in Ethnic Russian Cystic Fibrosis Patients
Nika Petrova et al.
GENES (2020)
The Changing Epidemiology of Cystic Fibrosis: Incidence, Survival and Impact of the CFTR Gene Discovery
Virginie Scotet et al.
GENES (2020)
KIR Variation in Iranians Combines High Haplotype and Allotype Diversity With an Abundance of Functional Inhibitory Receptors
Claudia Alicata et al.
FRONTIERS IN IMMUNOLOGY (2020)
Health Status in the Islamic Republic of Iran, Middle East and North Africa Countries: Implications for Global Health
Hossein MIRZAEI et al.
Iranian Journal of Public Health (2020)
Phenotypic spectrum and genetic heterogeneity of cystic fibrosis in Sri Lanka
Neluwa Liyanage Ruwan Indika et al.
BMC MEDICAL GENETICS (2019)
Iranome: A catalog of genomic variations in the Iranian population
Zohreh Fattahi et al.
HUMAN MUTATION (2019)
Novel, rare and common pathogenic variants in the CFTR gene screened by high-throughput sequencing technology and predicted by in silico tools
Stephanie Villa-Nova Pereira et al.
SCIENTIFIC REPORTS (2019)
Distinct genetic variation and heterogeneity of the Iranian population
Zohreh Mehrjoo et al.
PLOS GENETICS (2019)
Epidemiology of CF: How registries can be used to advance our understanding of the CF population
Abaigeal D. Jackson et al.
JOURNAL OF CYSTIC FIBROSIS (2018)
Diagnosis of Cystic Fibrosis: Consensus Guidelines from the Cystic Fibrosis Foundation
Philip M. Farrell et al.
JOURNAL OF PEDIATRICS (2017)
Assessment of the Potential Distance of Dispersal of High Pathogenicity Avian Influenza Virus by Wild Mallards
Krzysztof Śmietanka et al.
AVIAN DISEASES (2016)
The Spectrum of CFTR Variants in Nonwhite Cystic Fibrosis Patients Implications for Molecular Diagnostic Testing
Iris Schrijver et al.
JOURNAL OF MOLECULAR DIAGNOSTICS (2016)
Mutation and new polymorphisms insight in introns 11 to 14a of CFTR gene of northern Iranian cystic fibrosis patients
Mohammad Reza Esmaeili Dooki et al.
GENE (2015)
Distribution of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Mutations in a Cohort of Patients Residing in Palestine
Issa Siryani et al.
PLOS ONE (2015)
Cystic fibrosis
Felix Ratjen et al.
NATURE REVIEWS DISEASE PRIMERS (2015)
Clinical presentation of mild cystic fibrosis in a Serbian patient homozygous for the CFTR mutation c.1393-1G>A
Aleksandra Nikolic et al.
JOURNAL OF CYSTIC FIBROSIS (2014)
CFTR Mutations Spectrum and the Efficiency of Molecular Diagnostics in Polish Cystic Fibrosis Patients
Ewa Zietkiewicz et al.
PLOS ONE (2014)
Beta-Thalassemia in Iran: New Insight into the Role of Genetic Admixture and Migration
Ali Reza Rezaee et al.
SCIENTIFIC WORLD JOURNAL (2012)
Cystic fibrosis in Chilean patients: Analysis of 36 common CFTR gene mutations
Guillermo Lay-Son et al.
JOURNAL OF CYSTIC FIBROSIS (2011)
Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations
Nejat Mahdieh et al.
JOURNAL OF HUMAN GENETICS (2010)
Common mutations in cuban cystic fibrosis patients
Teresa Collazo et al.
Journal of Cystic Fibrosis (2009)
Analysis of the CFTR gene in Iranian cystic fibrosis patients: Identification of eight novel mutations
Reza Alibakhshi et al.
JOURNAL OF CYSTIC FIBROSIS (2008)
The prevalence of cystic fibrosis in the European Union
Philip M. Farrell
JOURNAL OF CYSTIC FIBROSIS (2008)
Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice
C. Castellani et al.
JOURNAL OF CYSTIC FIBROSIS (2008)
CFTR gene analysis in Latin American CF patients:: Heterogeneous origin and distribution of mutations across the continent
Martin M. Perez et al.
JOURNAL OF CYSTIC FIBROSIS (2007)
A haplotype framework for cystic fibrosis mutations in Iran
E Elahi et al.
JOURNAL OF MOLECULAR DIAGNOSTICS (2006)
Rare CFTR mutation 1525-1G>A in a Pakistani patient
A Wahab et al.
JOURNAL OF TROPICAL PEDIATRICS (2004)
Spectrum of cystic fibrosis mutations in Serbia and Montenegro and strategy for prenatal diagnosis
D Radivojevic et al.
GENETIC TESTING (2004)
Transcript analysis of the cystic fibrosis splicing mutation 1525-1G>A shows use of multiple alternative splicing sites and suggests a putative role of exonic splicing enhancers -: art. no. e88
AS Ramalho et al.
JOURNAL OF MEDICAL GENETICS (2003)
Cystic fibrosis transmembrane regulator gene mutations in Bahrain
HA Eskandarani
JOURNAL OF TROPICAL PEDIATRICS (2002)
Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification
JP Schouten et al.
NUCLEIC ACIDS RESEARCH (2002)
Cystic fibrosis: A worldwide analysis of CFTR mutations - Correlation with incidence data and application to screening
JL Bobadilla et al.
HUMAN MUTATION (2002)
Cystic fibrosis mutations and associated haplotypes in Turkish cystic fibrosis patients
T Onay et al.
HUMAN BIOLOGY (2001)
Share Paper
