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Page 1
Clinical Manifestations of Various Molecular Cytogenetic Variants of Eight Cases of "8p Inverted Duplication/Deletion Syndrome".
Biomedicines. 2022 Feb 28;10(3):567. doi: 10.3390/biomedicines10030567.
Biomedicines. 2022.
PMID: 35327368
Free PMC article.
A new case of 17p13.3p13.1 microduplication resulted from unbalanced translocation: clinical and molecular cytogenetic characterization.
Markova ZG, Minzhenkova ME, Bessonova LA, Shilova NV.
Markova ZG, et al. Among authors: minzhenkova me.
Mol Cytogenet. 2021 Aug 31;14(1):41. doi: 10.1186/s13039-021-00562-1.
Mol Cytogenet. 2021.
PMID: 34465353
Free PMC article.
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Complex Chromosomal Rearrangement Involving Chromosomes 10 and 11, Accompanied by Two Adjacent 11p14.1p13 and 11p13p12 Deletions, Identified in a Patient with WAGR Syndrome.
Marakhonov AV, Vasilyeva TA, Minzhenkova ME, Sukhanova NV, Sparber PA, Andreeva NA, Teleshova MV, Baybagisova FK, Shilova NV, Kutsev SI, Zinchenko RA.
Marakhonov AV, et al. Among authors: minzhenkova me.
Int J Mol Sci. 2023 Nov 29;24(23):16923. doi: 10.3390/ijms242316923.
Int J Mol Sci. 2023.
PMID: 38069245
Free PMC article.
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Epidemiology of PAX6 Gene Pathogenic Variants and Expected Prevalence of PAX6-Associated Congenital Aniridia across the Russian Federation: A Nationwide Study.
Vasilyeva TA, Marakhonov AV, Voskresenskaya AA, Kadyshev VV, Sukhanova NV, Minzhenkova ME, Shilova NV, Latyshova AA, Ginter EK, Kutsev SI, Zinchenko RA.
Vasilyeva TA, et al. Among authors: minzhenkova me.
Genes (Basel). 2023 Nov 4;14(11):2041. doi: 10.3390/genes14112041.
Genes (Basel). 2023.
PMID: 38002984
Free PMC article.
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Newborn Screening for Severe T and B Cell Lymphopenia Using TREC/KREC Detection: A Large-Scale Pilot Study of 202,908 Newborns.
Marakhonov AV, Efimova IY, Mukhina AA, Zinchenko RA, Balinova NV, Rodina Y, Pershin D, Ryzhkova OP, Orlova AA, Zabnenkova VV, Cherevatova TB, Beskorovainaya TS, Shchagina OA, Polyakov AV, Markova ZG, Minzhenkova ME, Shilova NV, Larin SS, Khadzhieva MB, Dudina ES, Kalinina EV, Mudaeva DA, Saydaeva DH, Matulevich SA, Belyashova EY, Yakubovskiy GI, Tebieva IS, Gabisova YV, Irinina NA, Nurgalieva LR, Saifullina EV, Belyaeva TI, Romanova OS, Voronin SV, Shcherbina A, Kutsev SI.
Marakhonov AV, et al. Among authors: minzhenkova me.
J Clin Immunol. 2024 Apr 5;44(4):93. doi: 10.1007/s10875-024-01691-z.
J Clin Immunol. 2024.
PMID: 38578360
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A sporadic case of congenital aniridia caused by pericentric inversion inv(11)(p13q14) associated with a 977 kb deletion in the 11p13 region.
Vasilyeva TA, Marakhonov AV, Minzhenkova ME, Markova ZG, Petrova NV, Sukhanova NV, Koshkin PA, Pyankov DV, Kanivets IV, Korostelev SA, Krynskaya IA, Shilova NV, Kutsev SI, Kadyshev VV, Zinchenko RA.
Vasilyeva TA, et al. Among authors: minzhenkova me.
BMC Med Genomics. 2020 Sep 18;13(Suppl 8):130. doi: 10.1186/s12920-020-00790-1.
BMC Med Genomics. 2020.
PMID: 32948199
Free PMC article.
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