Primary microcephaly case from the Karachay-Cherkess Republic poses an additional support for microcephaly and Seckel syndrome spectrum disorders

por Marakhonov, Andrey V., Konovalov, Fedor A., Makaov, Amin Kh., Vasilyeva, Tatyana A., Kadyshev, Vitaly V., Galkina, Varvara A., Dadali, Elena L., Kutsev, Sergey I., Zinchenko, Rena A.
Publicado 2018

Analysis of CFTR Mutation Spectrum in Ethnic Russian Cystic Fibrosis Patients

por Petrova, Nika V., Kashirskaya, Nataliya Y., Vasilyeva, Tatyana A., Kondratyeva, Elena I., Zhekaite, Elena K., Voronkova, Anna Y., Sherman, Victoria D., Galkina, Varvara A., Ginter, Eugeny K., Kutsev, Sergey I., Marakhonov, Andrey V., Zinchenko, Rena A.
Publicado 2020

Epidemiology of Hereditary Diseases in the Karachay-Cherkess Republic

por Zinchenko, Rena A., Makaov, Amin Kh., Marakhonov, Andrey V., Galkina, Varvara A., Kadyshev, Vitaly V., El’chinova, Galina I., Dadali, Elena L., Mikhailova, Lyudmila K., Petrova, Nika V., Petrina, Nina E., Vasilyeva, Tatyana A., Gundorova, Polina, Polyakov, Alexander V., Alexandrova, Oksana Y., Kutsev, Sergey I., Ginter, Eugeny K.
Publicado 2020