نتایج جستجو برای: congenital bilateral absence of vas deferens cbavd

تعداد نتایج: 21192810  

Journal: :The Kaohsiung Journal of Medical Sciences 2008

Journal: :Respiratory Research 2001
Peadar G Noone Michael R Knowles

Cystic fibrosis is a genetic disease that is associated with abnormal sweat electrolytes, sino-pulmonary disease, exocrine pancreatic insufficiency, and male infertility. Insights into genotype/phenotype relations have recently been gained in this disorder. The strongest relationship exists between 'severe' mutations in the gene that encodes the cystic fibrosis transmembrane regulator (CFTR) an...

Journal: :Clinical chemistry 1998
C Gelfi M Perego P G Righetti S Cainarca S Firpo M Ferrari L Cremonesi

The poly-T tract in intron 8 of the cystic fibrosis conductance transmembrane regulator (CFTR) gene exists in three variants, 5T, 7T, and 9T. The 7T and 9T variants generate a predominantly normal transcript, whereas the 5T variant engenders an anomalous product. The analysis of the poly-T tract is assuming increasing relevance, both to assess the implication of the CFTR gene in congenital bila...

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