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[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: zolotukhina tv. Genetika. 2014 May;50(5):602-10. Genetika. 2014. PMID: 25715476 Russian.
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. Among authors: zolotukhina tv. Sex Dev. 2009;3(4):183-7. doi: 10.1159/000228718. Epub 2009 Sep 11. Sex Dev. 2009. PMID: 19752597
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. Among authors: zolotukhina tv. 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
39 results