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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.
J Clin Immunol. 2024 Apr 5;44(4):93. doi: 10.1007/s10875-024-01691-z.
J Clin Immunol. 2024.
PMID: 38578360
Pathogenic Variants and Genotypes of the CFTR Gene in Russian Men with Cystic Fibrosis and CBAVD Syndrome.
Chernykh V, Krasovsky S, Solovova O, Adyan T, Stepanova A, Marnat E, Shtaut M, Sedova A, Sorokina T, Beskorovainaya T, Kondratyeva E, Shchagina O, Polyakov A.
Chernykh V, et al. Among authors: beskorovainaya t.
Int J Mol Sci. 2023 Nov 14;24(22):16287. doi: 10.3390/ijms242216287.
Int J Mol Sci. 2023.
PMID: 38003474
Free PMC article.
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Case Report: Complicated Molecular Diagnosis of MECP2 Gene Structural Rearrangement in a Proband with Rett Syndrome.
Beskorovainaya T, Konovalov F, Demina N, Shchagina O, Pashchenko M, Kanivets I, Pyankov D, Ryzhkova O, Polyakov A.
Beskorovainaya T, et al.
J Autism Dev Disord. 2021 Jun;51(6):2159-2163. doi: 10.1007/s10803-020-04668-0.
J Autism Dev Disord. 2021.
PMID: 32816169
No abstract available.
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A Family Case of Congenital Myasthenic Syndrome-22 Induced by Different Combinations of Molecular Causes in Siblings.
Shchagina O, Bessonova L, Bychkov I, Beskorovainaya T, Poliakov A.
Shchagina O, et al. Among authors: beskorovainaya t.
Genes (Basel). 2020 Jul 19;11(7):821. doi: 10.3390/genes11070821.
Genes (Basel). 2020.
PMID: 32707643
Free PMC article.
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