Frequency of cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in azoospermic Egyptian patients

Role of cystic fibrosis transmembrane conductance regulator gene in azoospermic patients with congenital bilateral absence of the vas deferens in Egypt

Genetic Mutations and Major Human Disorders: A Review

MOLECULAR GENETIC AND LABORATORY FINDINGS IN INFERTILE MEN WITH NON-OBSTRUCTIVE AZOOSPERMIA

Biochemical, Molecular and Genetic Studies on Human Male Fertility

An update on non-obstructive azoospermia; a narrative review

Association of the Role MTHFR 677C>T and 1298A>C polymorphisms variants as the risk factor with human male infertility.

Clinical versus Genetic Diagnosis of Cystic Fibrosis in High Risk Egyptian Children

Mutations in the Methylenetetrahydrofolate Reductase Gene and Methionine Metabolism in male infertility

Azoospermia Factors Microdeletion and Correlation to Male Infertility: An Egyptian Study