V. Zabnenkova

发表

Heterozygous carrier rate for type I–IV proximal spinal muscular atrophy in Chuvashes, Udmurts, and residents of the Moscow region

M. Spiridonova, E. Dadali, A. Polyakov, 2012, Russian Journal of Genetics.

SMN1 gene point mutations in type I–IV proximal spinal muscular atrophy patients with a single copy of SMN1

E. Dadali, A. Polyakov, G. Rudenskaya, 2015, Russian Journal of Genetics.

HTT Gene Premutation Allele Frequencies in the Russian Federation

S. Kopishinskaya, O. Schagina, A. Polyakov, 2018, Russian Journal of Genetics.

Hemophilia B Leyden: Literature and Our Data

A. Polyakov, O. Shchagina, R. Zinchenko, 2021, Russian Journal of Genetics.

Geneticl and clinical characteristics of 22q11.2 deletion syndrome

I. Kazantseva, A. Polyakov, T. V. Zolotukhina, 2014, Russian Journal of Genetics.

Heterozygous carrier rate for type I–IV proximal spinal muscular atrophy in Chuvashes, Udmurts, and residents of the Moscow region

M. Spiridonova, E. Dadali, A. Polyakov, 2012, Russian Journal of Genetics.

SMN1 gene point mutations in type I–IV proximal spinal muscular atrophy patients with a single copy of SMN1

E. Dadali, A. Polyakov, G. Rudenskaya, 2015, Russian Journal of Genetics.

HTT Gene Premutation Allele Frequencies in the Russian Federation

S. Kopishinskaya, O. Schagina, A. Polyakov, 2018, Russian Journal of Genetics.

Identification of large deletions in the APC gene in Russian patients with familial adenomatous polyposis.

A. Polyakov, V. Shubin, S. Frolov, 2020, Neoplasma.