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Update of the GJB2/DFNB1 mutation spectrum in Russia: a founder Ingush mutation del(GJB2-D13S175) is the most frequent among other large deletions.

Autor: Bliznetz EA; The Federal Agency for Scientific Organizations, Federal State Budgetary Institution, Research Centre for Medical Genetics, Moscow, Russia., Lalayants MR; Federal Medical and Biological Agency, Federal State-Funded Institution of Science, National Research Center for Audiology and Hearing Rehabilitation, Moscow, Russia., Markova TG; Federal Medical and Biological Agency, Federal State-Funded Institution of Science, National Research Center for Audiology and Hearing Rehabilitation, Moscow, Russia., Balanovsky OP; The Federal Agency for Scientific Organizations, Federal State Budgetary Institution, Research Centre for Medical Genetics, Moscow, Russia.; The Russian Academy of Sciences, Federal State-Funded Institution of Science, Vavilov Institute of General Genetics, Moscow, Russia., Balanovska EV; The Federal Agency for Scientific Organizations, Federal State Budgetary Institution, Research Centre for Medical Genetics, Moscow, Russia., Skhalyakho RA; The Federal Agency for Scientific Organizations, Federal State Budgetary Institution, Research Centre for Medical Genetics, Moscow, Russia.; The Russian Academy of Sciences, Federal State-Funded Institution of Science, Vavilov Institute of General Genetics, Moscow, Russia., Pocheshkhova EA; The Ministry of Health, Federal State-Funded Educational Institution of Higher Education, Kuban State Medical University, Krasnodar, Russia., Nikitina NV; The Ministry of Health, State Budgetary Healthcare Institution, Clinical-Diagnostic Center of Mother and Child Health Protection, Yekaterinburg, Russia., Voronin SV; State Autonomous Healthcare Institution, Regional Clinical Center of Specialized Medical Care, Vladivostok, Russia., Kudryashova EK; The Ministry of Health, State Budgetary Healthcare Institution, Leningrad Regional Clinical Hospital, Saint Petersburg, Russia., Glotov OS; Federal State Budgetary Educational Institution of Higher Education, Saint Petersburg University, Saint Petersburg, Russia., Polyakov AV; The Federal Agency for Scientific Organizations, Federal State Budgetary Institution, Research Centre for Medical Genetics, Moscow, Russia.

Publikováno v: Journal of human genetics [J Hum Genet] 2017 Aug; Vol. 62 (8), pp. 789-795. Date of Electronic Publication: 2017 Apr 13.

Polymorphisms of D1 S80 and 3'ApoB minisatellite loci in Northern Caucasus populations.

Autor: Verbenko DA; Human Molecular Genetics Dept, Institute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russia. dav@img.ras.ru, Pocheshkhova EA, Balanovskaya EV, Marshanija EZ, Kvitzinija PK, Limborska SA

Publikováno v: Journal of forensic sciences [J Forensic Sci] 2004 Jan; Vol. 49 (1), pp. 178-80.

[Genogeographic analysis of subdivided population. The Adyge gene pool in the Caucasian gene pool system].

Autor: Balanovskaia EV; Medical Genetic Research Center, Russian Academy of Medical Sciences, Moscow, Russia., Nurbaev SD, Balanovskiĭ OP, Pocheshkhova EA, Borovinskikh AA, Ginter EK

Publikováno v: Genetika [Genetika] 1999 Jun; Vol. 35 (6), pp. 818-30.