Образовательная политика. Российская академия народного хозяйства и государственной службы при Президенте РФ. 2019. С. 132-141
Aim: To identify the main genetic causes of azoospermia. Methods. The study included 92 patients with azoospermia. In all patients we carried out genetic tests - karyotyping, PCRdiagnosis of blood. Results. Genetic disorders were found in 35 (38%) men. Of these, the majority of men were with Kleinfelter syndrome - 21 (60%) and deletions in the AZF regions of the Y chromosome - 11 (31.4%). Conclusions. Patients who have genetic abnormalities should receive comprehensive medical and genetic advice.