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Page 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: antonenko vg. Genetika. 2014 May;50(5):602-10. Genetika. 2014. PMID: 25715476 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. Among authors: antonenko vg. 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 new case of trisomy 5p].
Antonenko VG, Levina LIa, Chudnova VI. Antonenko VG, et al. Genetika. 1985 Dec;21(12):2066-70. Genetika. 1985. PMID: 4085794 Russian.
[Study of CATCH 22: genetic aspects].
Antonenko VG, Ivanov VI, Konstantinova LM, Levina LIa, Mglinets VA. Antonenko VG, et al. Vestn Ross Akad Med Nauk. 2000;(5):46-50. Vestn Ross Akad Med Nauk. 2000. PMID: 10881663 Review. Russian.
[Our experience with 2220 stereotaxic operations].
Laponogov OA, Tsymbaliuk VI, Matiuk NG, Rymar' VV, Antonenko VG, Melendez KhA. Laponogov OA, et al. Among authors: antonenko vg. Zh Vopr Neirokhir Im N N Burdenko. 1990 Jan-Feb;(1):17-9. Zh Vopr Neirokhir Im N N Burdenko. 1990. PMID: 2164296 Russian.
12 results