Screening of ΔF508 mutation and IVS8‐poly T polymorphism in CFTR gene in Tunisian infertile men without CBAVD
M Ghorbel, S Baklouti‐Gargouri, R Keskes… - Andrologia, 2012 - Wiley Online Library
It is well established that cystic fibrosis transmembrane conductance regulator gene (CFTR)
mutations are involved in congenital bilateral absence of the vas deferens (CBAVD) …
mutations are involved in congenital bilateral absence of the vas deferens (CBAVD) …
Screening of ΔF508 mutation and IVS8-poly T polymorphism in CFTR gene in Tunisian infertile men without CBAVD.
M Ghorbel, S Baklouti-Gargouri, R Keskes… - 2012 - cabidigitallibrary.org
It is well established that cystic fibrosis transmembrane conductance regulator gene (CFTR)
mutations are involved in congenital bilateral absence of the vas deferens (CBAVD) …
mutations are involved in congenital bilateral absence of the vas deferens (CBAVD) …
Screening of ΔF508 mutation and IVS8-poly T polymorphism in CFTR gene in Tunisian infertile men without CBAVD
M Ghorbel, S Baklouti-Gargouri, R Keskes… - …, 2012 - pubmed.ncbi.nlm.nih.gov
It is well established that cystic fibrosis transmembrane conductance regulator gene (CFTR)
mutations are involved in congenital bilateral absence of the vas deferens (CBAVD) …
mutations are involved in congenital bilateral absence of the vas deferens (CBAVD) …
Screening of ΔF508 mutation and IVS8-poly T polymorphism in CFTR gene in Tunisian infertile men without CBAVD.
M Ghorbel, S Baklouti-Gargouri, R Keskes… - Andrologia, 2011 - europepmc.org
It is well established that cystic fibrosis transmembrane conductance regulator gene (CFTR)
mutations are involved in congenital bilateral absence of the vas deferens (CBAVD) …
mutations are involved in congenital bilateral absence of the vas deferens (CBAVD) …
Screening of ΔF508 mutation and IVS8-poly T polymorphism in CFTR gene in Tunisian infertile men without CBAVD.
M Ghorbel, S Baklouti-Gargouri, R Keskes… - …, 2012 - search.ebscohost.com
It is well established that cystic fibrosis transmembrane conductance regulator gene (CFTR)
mutations are involved in congenital bilateral absence of the vas deferens (CBAVD) …
mutations are involved in congenital bilateral absence of the vas deferens (CBAVD) …
Screening of ΔF508 mutation and IVS8‐poly T polymorphism in CFTR gene in Tunisian infertile men without CBAVD
M Ghorbel, S Baklouti‐Gargouri, R Keskes… - Andrologia, 2012 - infona.pl
It is well established that cystic fibrosis transmembrane conductance regulator gene (CFTR)
mutations are involved in congenital bilateral absence of the vas deferens (CBAVD) …
mutations are involved in congenital bilateral absence of the vas deferens (CBAVD) …