Introduction: Cystic fibrosis (CF) is the most frequent autosomical recessive disorder in Caucasian population with an incidence of 1 in 2000 newborns. The disease is caused by mutations in the cftr gene, but the most common mutation is F508del, which accounts for 66% of CF chromosomes worldwide and a carrier frequency for Caucasian population of 1 in 25. Objective: To determine the carrier frequency of the F508del mutation in 110 unrelated, healthy students from the Facultad de Medicina, Universidad del Rosario. Methods: The presence of F508del mutation using PCR and heteroduplex analysis was determined. Results: Only four heterozygotes for F508del mutation were discovered. This represents a carrier frequency of 1 in 27 students. Conclusio...
We have initiated the screening of the delta F508 cystic fibrosis (CF) mutation in our country basin...
Cystic fibrosis (CF) is the most common genetic disease among Caucasians and is rare among sub-Sahar...
Fil: Pérez, Martín M. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica; Argentina.Fil: Luna,...
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...
Background: Cystic fibrosis (CF) is the most frequent autosomal recessive disorder in the Caucasian ...
We analyzed 192 cystic fibrosis (CF) alleles in three Latin American countries: Mexico, Colombia, an...
La fibrosis quística es la enfermedad letal autosómica recesiva más frecuente en caucásicos, donde s...
La Fibrosis Quística (FQ) es la enfermedad autosómica recesiva más común en la población Caucásica, ...
PURPOSE: To analyze the frequency of the delta F508 (deltaF508) deletion mutation in 108 unrelated c...
BACKGROUND: Cystic Fibrosis (CF) is the most prevalent Mendelian disorder in European populations. D...
We conducted clinical and genetic analyses of 52 cystic fibrosis (CF) patients in Uruguay, which is ...
Congenital bilateral absence of the vas deferens (CBAVD) is a form of male infertility in which muta...
ABSTRACT. Cystic fibrosis is the most common hereditary disease in populations of European descent, ...
Cystic fibrosis (CF) is the most common autosomal recessive disease of the Caucasian population. Amo...
We have initiated the screening of the delta F508 cystic fibrosis (CF) mutation in our country basin...
Cystic fibrosis (CF) is the most common genetic disease among Caucasians and is rare among sub-Sahar...
Fil: Pérez, Martín M. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica; Argentina.Fil: Luna,...
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...
Background: Cystic fibrosis (CF) is the most frequent autosomal recessive disorder in the Caucasian ...
We analyzed 192 cystic fibrosis (CF) alleles in three Latin American countries: Mexico, Colombia, an...
La fibrosis quística es la enfermedad letal autosómica recesiva más frecuente en caucásicos, donde s...
La Fibrosis Quística (FQ) es la enfermedad autosómica recesiva más común en la población Caucásica, ...
PURPOSE: To analyze the frequency of the delta F508 (deltaF508) deletion mutation in 108 unrelated c...
BACKGROUND: Cystic Fibrosis (CF) is the most prevalent Mendelian disorder in European populations. D...
We conducted clinical and genetic analyses of 52 cystic fibrosis (CF) patients in Uruguay, which is ...
Congenital bilateral absence of the vas deferens (CBAVD) is a form of male infertility in which muta...
ABSTRACT. Cystic fibrosis is the most common hereditary disease in populations of European descent, ...
Cystic fibrosis (CF) is the most common autosomal recessive disease of the Caucasian population. Amo...
We have initiated the screening of the delta F508 cystic fibrosis (CF) mutation in our country basin...
Cystic fibrosis (CF) is the most common genetic disease among Caucasians and is rare among sub-Sahar...
Fil: Pérez, Martín M. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica; Argentina.Fil: Luna,...