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Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome Sequencing.
Lebedev IN, Karamysheva TV, Elisaphenko EA, Makunin AI, Zhigalina DI, Lopatkina ME, Drozdov GV, Cheremnykh AD, Torkhova NB, Seitova GN, Vasilyev SA, Kashevarova AA, Nazarenko LP, Rubtsov NB. Lebedev IN, et al. Among authors: cheremnykh ad. Biomedicines. 2021 Aug 17;9(8):1030. doi: 10.3390/biomedicines9081030. Biomedicines. 2021. PMID: 34440234 Free PMC article.
[Clinical and genetic analysis of idiopathic intellectual disability based on array comparative genomic hybridization].
Kashevarova AA, Skryabin NA, Cheremnykh AD, Tolmacheva EN, Sazhenova EA, Salyukova OA, Chechetkina NN, Didenko LI, Sukhanova NN, Yakovleva YS, Torkhova NB, Nazarenko LP, Magini P, Graziano C, Romeo G, Lebedev IN. Kashevarova AA, et al. Among authors: cheremnykh ad. Zh Nevrol Psikhiatr Im S S Korsakova. 2013;113(9):70-4. Zh Nevrol Psikhiatr Im S S Korsakova. 2013. PMID: 24107884 Russian.
A case report of Pallister-Killian syndrome with an unusual mosaic supernumerary marker chromosome 12 with interstitial 12p13.1-p12.1 duplication.
Karamysheva TV, Lebedev IN, Minaycheva LI, Nazarenko LP, Kashevarova AA, Fedotov DA, Skryabin NA, Lopatkina ME, Cheremnykh AD, Fonova EA, Nikitina TV, Sazhenova EA, Skleimova MM, Kolesnikov NA, Drozdov GV, Yakovleva YS, Seitova GN, Orishchenko KE, Rubtsov NB. Karamysheva TV, et al. Among authors: cheremnykh ad. Front Genet. 2024 Mar 11;15:1331066. doi: 10.3389/fgene.2024.1331066. eCollection 2024. Front Genet. 2024. PMID: 38528911 Free PMC article.