O. Makienko

Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome

Viktoriia Zabnenkova, O. Shchagina, O. Makienko, 2022, The application of clinical genetics.

New recurrent large deletion, encompassing both GJB2 and GB6 genes, results in isolated sensorineural hearing impairment with autosomal recessive mode of inheritance

A. Polyakov, O. Makienko, E. G. Okuneva, 2014, Russian Journal of Genetics.

TACG_A_342804 1..10

Viktoriia Zabnenkova, O. Shchagina, O. Makienko, 2022 .

New recurrent large deletion, encompassing both GJB2 and GB6 genes, results in isolated sensorineural hearing impairment with autosomal recessive mode of inheritance

A. Polyakov, O. Makienko, E. G. Okuneva, 2014, Russian Journal of Genetics.