Background: Cystic fibrosis (CF) is the most frequent autosomal recessive disorder in the Caucasian population with an incidence of 1 in 2,500 newborns. More than 1,300 mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene that causes CF have been described. However, mutation F508del is the most common mutation in different populations around the world. Objective: To develop a fast, reliable and low-cost technique to screen carriers and affected individuals for the F508del mutation. This kind of analysis will have an impact on genetic counselling to decrease the incidence of new cases, in the early diagnosis and instauration of appropriate treatment to decrease morbidity and mortality associated to CF in Colombia....
Cystic fibrosis (CF), an autosomal recessive genetic disease, is recognized as one of the most preva...
We have initiated the screening of the delta F508 cystic fibrosis (CF) mutation in our country basin...
Background: High heterogeneity levels of cystic fibrosis transmembrane regulator (CFTR) are manifest...
Background: Cystic fibrosis (CF) is the most frequent autosomal recessive disorder in the Caucasian ...
Introduction: Cystic fibrosis (CF) is the most frequent autosomical recessive disorder in Caucasian ...
Introduction: Cystic fibrosis (CF) is the most frequent autosomical recessive disorder in Caucasian ...
Introducción: La fibrosis quística es la enfermedad letal autosómica recesiva más frecuente en caucá...
We analyzed 192 cystic fibrosis (CF) alleles in three Latin American countries: Mexico, Colombia, an...
Abstract Background Mutation scanning methods in Cystic Fibrosis Transmembrane Conductance Regulator...
As a contribution to establish the real incidence of cystic fibrosis (CF) and the prevalent mutation...
Cystic fibrosis (CF), which is due to mutations in the cystic fibrosis transmembrane conductance reg...
Introduction: Cystic fibrosis is an autosomal recessive genetic disease classified as a highcost orp...
Cystic fibrosis (CF) is the most common autosomal recessive disease of the Caucasian population. Amo...
We have analyzed 97 CF unrelated Mexican families for mutations in the cystic fibrosis transmembrane...
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Objective: To determine the relevance o...
Cystic fibrosis (CF), an autosomal recessive genetic disease, is recognized as one of the most preva...
We have initiated the screening of the delta F508 cystic fibrosis (CF) mutation in our country basin...
Background: High heterogeneity levels of cystic fibrosis transmembrane regulator (CFTR) are manifest...
Background: Cystic fibrosis (CF) is the most frequent autosomal recessive disorder in the Caucasian ...
Introduction: Cystic fibrosis (CF) is the most frequent autosomical recessive disorder in Caucasian ...
Introduction: Cystic fibrosis (CF) is the most frequent autosomical recessive disorder in Caucasian ...
Introducción: La fibrosis quística es la enfermedad letal autosómica recesiva más frecuente en caucá...
We analyzed 192 cystic fibrosis (CF) alleles in three Latin American countries: Mexico, Colombia, an...
Abstract Background Mutation scanning methods in Cystic Fibrosis Transmembrane Conductance Regulator...
As a contribution to establish the real incidence of cystic fibrosis (CF) and the prevalent mutation...
Cystic fibrosis (CF), which is due to mutations in the cystic fibrosis transmembrane conductance reg...
Introduction: Cystic fibrosis is an autosomal recessive genetic disease classified as a highcost orp...
Cystic fibrosis (CF) is the most common autosomal recessive disease of the Caucasian population. Amo...
We have analyzed 97 CF unrelated Mexican families for mutations in the cystic fibrosis transmembrane...
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Objective: To determine the relevance o...
Cystic fibrosis (CF), an autosomal recessive genetic disease, is recognized as one of the most preva...
We have initiated the screening of the delta F508 cystic fibrosis (CF) mutation in our country basin...
Background: High heterogeneity levels of cystic fibrosis transmembrane regulator (CFTR) are manifest...