Poliakov AV - Search Results

1

[Genetic and clinical characteristics of 22q11.2 deletion syndrome].

Kozlova IuO, Zabnenkova VV, Shilova NV, Min'zhenkova ME, Antonenko VG, Kotlukova NP, Simonova LV, Kazanceva IA, Levchenko EG, Bombardirova TD, Zolotukhina TV, Poliakov AV. Kozlova IuO, et al. Among authors: poliakov av. Genetika. 2014 May;50(5):602-10. Genetika. 2014. PMID: 25715476 Russian.

2

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

Zabnenkova VV, Dadali EL, Spiridonova MG, Zinchenko RA, Poliakov AV. Zabnenkova VV, et al. Among authors: poliakov av. Genetika. 2012 Aug;48(8):983-92. Genetika. 2012. PMID: 23035550 Russian.

3

[Lamine gene mutations in dilated cardiomyopathy].

Zakliaz'minskaia EV, Chukhrova AL, Tverskaia SM, Rudenskaia GE, Treshkur TV, Gudkova AIa, Parmon EV, Kotlukova NP, Chapurnykh AV, Serebrennikova TE, Poliakov AV. Zakliaz'minskaia EV, et al. Among authors: poliakov av. Kardiologiia. 2005;45(2):47-52. Kardiologiia. 2005. PMID: 15798706 Russian. No abstract available.

4

[New recurrent extended deletion, including GJB2 and GJB6 genes, results in isolated sensorineural hearing impairment with autosomal recessive type of inheritance].

Bliznets EA, Makienko ON, Okuneva EG, Markova TG, Poliakov AV. Bliznets EA, et al. Among authors: poliakov av. Genetika. 2014 Apr;50(4):474-80. Genetika. 2014. PMID: 25715449 Russian.

5

[Screening for deletion in patients with Duchenne's myodystrophy by multiplex amplification].

Chukhrova AL, Malygina NA, Poliakov AV, Zaĭtseva SP, Sitnikov VF, Dadali EL, Kamennykh LN, Khrennikov VIu, Badalian LO, Evgrafov OV. Chukhrova AL, et al. Among authors: poliakov av. Tsitol Genet. 1994 Jul-Aug;28(4):80-3. Tsitol Genet. 1994. PMID: 7801388 Russian.

6

[Types of Y chromosome deletions and their frequency in infertile men].

Chernykh VB, Chukhrova AL, Beskorovaĭnaia TS, Grishina EM, Sorokina TM, Shileĭko LV, Gogolevskiĭ PA, Kalugina AS, Morina GV, Togobetskiĭ AS, Tanevskiĭ VE, Zdanovskiĭ VM, Gogolevskaia IK, Kramerov DA, Poliakov AV, Kurilo LF. Chernykh VB, et al. Among authors: poliakov av. Genetika. 2006 Aug;42(8):1130-6. Genetika. 2006. PMID: 17025164 Russian.

7

[The mutation spectrum of the GJB2 gene in Belarussian patients with hearing loss. Results of pilot genetic screening of hearing impairment in newborns].

Bliznets EA, Marcul' DN, Khorov OG, Markova TG, Poliakov AV. Bliznets EA, et al. Among authors: poliakov av. Genetika. 2014 Feb;50(2):214-21. Genetika. 2014. PMID: 25711030 Russian.

8

[Molecular analysis of the Y chromosome in XX sex-reversed patients].

Chernykh VB, Chukhrova AL, Vasserman NN, Il'ina EV, Karmanov ME, Fedotov VP, Poliakov AV. Chernykh VB, et al. Among authors: poliakov av. Genetika. 2008 Feb;44(2):236-41. Genetika. 2008. PMID: 18619043 Russian.

9

[Novel large deletion c.22-1320_633+1224del in the CYB5R3 gene from patients with hereditary methemoglobinemia].

Galeeva NM, Nenasheva SA, Kleĭmenova IS, Poliakov AV. Galeeva NM, et al. Among authors: poliakov av. Genetika. 2012 Nov;48(11):1336-46. Genetika. 2012. PMID: 23297489 Russian.

10

[The spectrum of CLCN1 gene mutations in patients with nondystrophic Thomsen's and Becker's myotonias].

Ivanova EA, Dadali EL, Fedotov VP, Kurbatov SA, Rudenskaia GE, Proskokova TN, Poliakov AV. Ivanova EA, et al. Among authors: poliakov av. Genetika. 2012 Sep;48(9):1113-23. Genetika. 2012. PMID: 23113340 Russian.

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