predisposition to AP-induced LQTS may be due to several causes, including causal mutations in the genes

by marked polymorphism with variable severity of skeletal and extra-skeletal features. Previous studies have

of the brain. Changes in cerebral perfusion did not correlate with the degree of reduction in the severity

of the OGG1 gene and the severity of DNA breaks. The study revealed adverse effects produced by the chemical

Особенности системы гемостаза у беременных с гипертензивными расстройствами, проживающих в высокогорных условиях Республики Таджикистан,0 %) pregnant women, respectively, were diagnosed with severe preeclampsia. Hemostasis parameters were examined

Фенотипические проявления дисплазии соединительной ткани у лиц с гипермобильностью суставов in the control group (p = 0.020), and severe myopia was more common in the JH group (p = 0.003). Keloid scars