Author:
Khedri Azam,Farahmandi Amir Yousef,Moghaveleh Mohammad,Baghbani Kourosh Akbari,Khoob Saman Naddaf,Moghbelinejad Sahar,Asadi Fatemeh
Reference46 articles.
1. A unique view on male infertility around the globe;Agarwal;Reprod. Biol. Endocrinol.,2015
2. A survey of the common mutations and IVS8-Tn polymorphism of cystic fibrosis transmembrane conductance regulator gene in infertile men with nonobstructive azoospermia and CBAVD in Iranian;Asadi;Population.,2019
3. et al;Casals;Heterogeneity for mutations in the CFTR gene and clinical correlations in patients with congenital absence of the vas deferens.,2000
4. Extensive analysis of 40 infertile patients with congenital absence of the vas deferens: in 50% of cases only one CFTR allele could be detected;Casals;Hum. Genet.,1995
5. CFTR (TG) m (T) n polymorphism in patients with CBAVD in a population expressing low incidence of cystic fibrosis;Chiang;Clin. Genet.,2009