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Prenatal Identification of a Novel Mutation in the MCPH1 Gene Associated with Autosomal Recessive Primary Microcephaly (MCPH) Using Next Generation Sequencing (NGS): A Case Report and Review of the Literature.
Papoulidis I, Eleftheriades M, Manolakos E, Petersen MB, Liappi SM, Konstantinidou A, Papamichail M, Papadopoulos V, Garas A, Sotiriou S, Papastefanou I, Daskalakis G, Ristic A. Papoulidis I, et al. Among authors: garas a. Children (Basel). 2022 Nov 30;9(12):1879. doi: 10.3390/children9121879. Children (Basel). 2022. PMID: 36553323 Free PMC article.
The use of array-CGH in a cohort of Greek children with developmental delay.
Manolakos E, Vetro A, Kefalas K, Rapti SM, Louizou E, Garas A, Kitsos G, Vasileiadis L, Tsoplou P, Eleftheriades M, Peitsidis P, Orru S, Liehr T, Petersen MB, Thomaidis L. Manolakos E, et al. Among authors: garas a. Mol Cytogenet. 2010 Nov 9;3:22. doi: 10.1186/1755-8166-3-22. Mol Cytogenet. 2010. PMID: 21062444 Free PMC article.
Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridization.
Manolakos E, Kefalas K, Neroutsou R, Lagou M, Kosyakova N, Ewers E, Ziegler M, Weise A, Tsoplou P, Rapti SM, Papoulidis I, Anastasakis E, Garas A, Sotiriou S, Eleftheriades M, Peitsidis P, Malathrakis D, Thomaidis L, Kitsos G, Orru S, Liehr T, Petersen MB, Kitsiou-Tzeli S. Manolakos E, et al. Among authors: garas a. Mol Med Rep. 2010 Nov-Dec;3(6):1015-22. doi: 10.3892/mmr.2010.358. Epub 2010 Sep 10. Mol Med Rep. 2010. PMID: 21472348
Proximal 10q duplication in a child with severe central hypotonia characterized by array-comparative genomic hybridization: A case report and review of the literature.
Manolakos E, Vetro A, Garas A, Thomaidis L, Kefalas K, Kitsos G, Ziegler M, Liehr T, Zuffardi O, Papoulidis I. Manolakos E, et al. Among authors: garas a. Exp Ther Med. 2014 Apr;7(4):953-957. doi: 10.3892/etm.2014.1520. Epub 2014 Feb 6. Exp Ther Med. 2014. PMID: 24669257 Free PMC article.
7q Deletion/12q Duplication Is the Possible Cause of an Alobar Holoprosencephaly Case.
Paspaliaris V, Vrachnis N, Iliodromiti Z, Antonakopoulos N, Papaioannou G, Vlachadis N, Anastasiadou F, Sotiriou S, Garas A, Thomaidis L, Manolakos E. Paspaliaris V, et al. Among authors: garas a. Mol Syndromol. 2017 Dec;9(1):52-57. doi: 10.1159/000481972. Epub 2017 Nov 24. Mol Syndromol. 2017. PMID: 29456484 Free PMC article.
Association of maternal angiotensin II type 1 and type 2 receptor combination genotypes with susceptibility to early-onset preeclampsia.
Satra M, Samara M, Alatsathianos G, Vamvakopoulou D, Baka A, Tsalazidou-Founta TM, Sidiropoulos A, Vamvakopoulos KO, Garas A, Daponte A, Vamvakopoulos N, Sotiriou S. Satra M, et al. Among authors: garas a. J Hum Hypertens. 2022 Mar;36(3):271-279. doi: 10.1038/s41371-021-00524-5. Epub 2021 Mar 23. J Hum Hypertens. 2022. PMID: 33758348
77 results