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New Compound Heterozygous Splice Site Mutations of the Skeletal Muscle Ryanodine Receptor (RYR1) Gene Manifest Fetal Akinesia: A Linkage with Congenital Myopathies.
Zecevic N, Arsenijevic V, Manolakos E, Papoulidis I, Theocharis G, Sartsidis A, Tsagas T, Tziotis I, Dagklis T, Kalogeros G, Tsakiridis I, Filipovic Stankovic M, Eleftheriades M. Zecevic N, et al. Among authors: tsakiridis i. Mol Syndromol. 2020 Jun;11(2):104-109. doi: 10.1159/000507034. Epub 2020 Apr 1. Mol Syndromol. 2020. PMID: 32655342 Free PMC article.
Complex Rearrangement Involving Three Chromosomes, Four Breakpoints and a 2.7-Mb Deletion in the 18q Segment Observed in a Girl with Mild Learning Difficulties.
Kontodiou M, Daskalakis G, Vetro A, Paspaliaris V, Papaioannou G, Dagklis T, Tsakiridis I, Ziegler M, Liehr T, Thomaidis L, Papoulidis I, Manolakos E. Kontodiou M, et al. Among authors: tsakiridis i. Cytogenet Genome Res. 2015;147(2-3):118-23. doi: 10.1159/000442583. Epub 2015 Dec 18. Cytogenet Genome Res. 2015. PMID: 26681178
146 results