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Molecular landscape of congenital vertebral malformations: recent discoveries and future directions.
Orphanet J Rare Dis. 2024 Jan 30;19(1):32. doi: 10.1186/s13023-024-03040-0.
Orphanet J Rare Dis. 2024.
PMID: 38291488
Free PMC article.
Review.
A genotype-phenotype correlation in split-hand/foot malformation type 1: further refinement of the phenotypic subregions within the 7q21.3 locus.
Sowińska-Seidler A, Socha M, Szoszkiewicz A, Materna-Kiryluk A, Jamsheer A.
Sowińska-Seidler A, et al. Among authors: szoszkiewicz a.
Front Mol Biosci. 2023 Oct 17;10:1250714. doi: 10.3389/fmolb.2023.1250714. eCollection 2023.
Front Mol Biosci. 2023.
PMID: 37916192
Free PMC article.
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A pure de novo 16p13.3 duplication and amplification in a patient with femoral hypoplasia, psychomotor retardation, heart defect, and facial dysmorphism-a case report and literature review of the partial 16p13.3 trisomy syndrome.
Socha M, Szoszkiewicz A, Simon D, Jamsheer A.
Socha M, et al. Among authors: szoszkiewicz a.
J Appl Genet. 2023 Feb;64(1):125-134. doi: 10.1007/s13353-022-00743-7. Epub 2022 Dec 31.
J Appl Genet. 2023.
PMID: 36586055
Free PMC article.
Review.
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Lichen Secondary Metabolites Inhibit the Wnt/β-Catenin Pathway in Glioblastoma Cells and Improve the Anticancer Effects of Temozolomide.
Majchrzak-Celińska A, Kleszcz R, Studzińska-Sroka E, Łukaszyk A, Szoszkiewicz A, Stelcer E, Jopek K, Rucinski M, Cielecka-Piontek J, Krajka-Kuźniak V.
Majchrzak-Celińska A, et al. Among authors: szoszkiewicz a.
Cells. 2022 Mar 23;11(7):1084. doi: 10.3390/cells11071084.
Cells. 2022.
PMID: 35406647
Free PMC article.
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