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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.
Complex Diagnostics of Non-Specific Intellectual Developmental Disorder.
Levchenko O, Dadali E, Bessonova L, Demina N, Rudenskaya G, Matyushchenko G, Markova T, Anisimova I, Semenova N, Shchagina O, Ryzhkova O, Zinchenko R, Galkina V, Voinova V, Nagieva S, Lavrov A.
Levchenko O, et al.
Int J Mol Sci. 2022 Jul 14;23(14):7764. doi: 10.3390/ijms23147764.
Int J Mol Sci. 2022.
PMID: 35887114
Free PMC article.
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Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome.
Zabnenkova V, Shchagina O, Makienko O, Matyushchenko G, Ryzhkova O.
Zabnenkova V, et al.
Appl Clin Genet. 2022 Jan 6;15:1-10. doi: 10.2147/TACG.S342804. eCollection 2022.
Appl Clin Genet. 2022.
PMID: 35023948
Free PMC article.
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