I. Barkov

发表

In silico size selection is effective in reducing false positive NIPS cases of monosomy X that are due to maternal mosaic monosomy X

A. Goltsov, G. Sukhikh, D. Trofimov, 2017, Prenatal diagnosis.

Prenatal diagnosis of Prader‐Willi syndrome due to uniparental disomy with NIPS: Case report and literature review

A. Goltsov, G. Sukhikh, M. Kuznetsova, 2020, Molecular genetics & genomic medicine.

Comparative results of preimplantation genetic screening by array comparative genomic hybridization and new-generation sequencing

G. Sukhikh, E. Kulakova, D. Trofimov, 2017, Molecular Biology.

Current relevance of non-invasive prenatal study of cell-free fetal DNA in the mother’s blood and prospects for its application in mass screening of pregnant women in the Russian Federation

A. Glotov, I. Barkov, Elena Aleksandrovna Kalashnikova, 2021 .

Detection of chromosomal rearrangements in the short arms of chromosomes 4 and 12 as an example of a whole-genome approach to noninvasive prenatal testing

A. Goltsov, D. Rebrikov, M. Kuznetsova, 2019, Bulletin of Russian State Medical University.

Two Novel Mutations Associated With Ataxia-Telangiectasia Identified Using an Ion AmpliSeq Inherited Disease Panel

G. Sukhikh, O. Gusev, M. Kuznetsova, 2017, Front. Neurol..

Comparative results of preimplantation genetic screening by array comparative genomic hybridization and new-generation sequencing

G. Sukhikh, E. Kulakova, D. Trofimov, 2017, Molecular Biology.

Molecular diagnosis of tuberous sclerosis complex in fetuses and infants: an institutional case series

D. Degtyarev, D. Trofimov, J. Shubina, 2023, Journal of clinical pathology.

Comparative results of preimplantation genetic screening by array comparative genomic hybridization and new-generation sequencing

G. Sukhikh, E. Kulakova, D. Trofimov, 2017, Molecular Biology.