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Rare multiple congenital anomalies-hypotonia-seizures syndrome type 1 (MCAHS1) - the clinical and molecular summary.
Eur J Med Genet. 2023 Jan;66(1):104668. doi: 10.1016/j.ejmg.2022.104668. Epub 2022 Nov 13.
Eur J Med Genet. 2023.
PMID: 36384198
Results from Genetic Studies in Patients Affected with Craniosynostosis: Clinical and Molecular Aspects.
Bukowska-Olech E, Sowińska-Seidler A, Larysz D, Gawliński P, Koczyk G, Popiel D, Gurba-Bryśkiewicz L, Materna-Kiryluk A, Adamek Z, Szczepankiewicz A, Dominiak P, Glista F, Matuszewska K, Jamsheer A.
Bukowska-Olech E, et al. Among authors: glista f.
Front Mol Biosci. 2022 Apr 28;9:865494. doi: 10.3389/fmolb.2022.865494. eCollection 2022.
Front Mol Biosci. 2022.
PMID: 35591945
Free PMC article.
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