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Page 1
Hidden X chromosomal mosaicism in a 46,XX male.
Chernykh VB, Kurilo LF, Shilova NV, Zolotukhina TV, Ryzhkova OP, Bliznetz EA, Polyakov AV. Chernykh VB, et al. Sex Dev. 2009;3(4):183-7. doi: 10.1159/000228718. Epub 2009 Sep 11. Sex Dev. 2009. PMID: 19752597
[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. Genetika. 2006 Aug;42(8):1130-6. Genetika. 2006. PMID: 17025164 Russian.
Unique mosaic X/Y translocation/insertion in infant 45,X male.
Chernykh VB, Vyatkina SV, Antonenko VG, Shilova NV, Zolotukhina TV, Kurilo LF, Chukhrova AL, Polyakov AV. Chernykh VB, et al. Am J Med Genet A. 2008 Dec 15;146A(24):3195-7. doi: 10.1002/ajmg.a.32578. Am J Med Genet A. 2008. PMID: 19012335
A 3-year-old boy with ovotestes: gender reassignment and surgical management.
Raygorodskaya NY, Chernykh VB, Morozov DA, Olutoye OO, Bolotova NV, Averyanov AP, Maslyakova GN, Shilova NV, Zolotukhina TV. Raygorodskaya NY, et al. Among authors: chernykh vb. J Pediatr Endocrinol Metab. 2011;24(7-8):587-9. doi: 10.1515/jpem.2011.244. J Pediatr Endocrinol Metab. 2011. PMID: 21932607
L138ins Variant of the CFTR Gene in Russian Infertile Men.
Chernykh V, Sorokina T, Sedova A, Shtaut M, Solovova O, Marnat E, Adyan T, Beskorovaynaya T, Stepanova A, Shchagina O, Polyakov A. Chernykh V, et al. Genes (Basel). 2023 Jul 7;14(7):1407. doi: 10.3390/genes14071407. Genes (Basel). 2023. PMID: 37510311 Free PMC article.
21 results