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Page 1
Sonographic antenatal diagnosis of congenital dacryocystoceles.
Sotiriou S, Manolakos E, Peitsidis P, Garas A. Sotiriou S, et al. Among authors: manolakos e. J Clin Ultrasound. 2012 Jul-Aug;40(6):375-7. doi: 10.1002/jcu.21937. Epub 2012 May 19. J Clin Ultrasound. 2012. PMID: 22610614
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: manolakos e. Children (Basel). 2022 Nov 30;9(12):1879. doi: 10.3390/children9121879. Children (Basel). 2022. PMID: 36553323 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: manolakos e. Mol Syndromol. 2017 Dec;9(1):52-57. doi: 10.1159/000481972. Epub 2017 Nov 24. Mol Syndromol. 2017. PMID: 29456484 Free PMC article.
Interstitial deletion at 11q14.2-11q22.1 may cause severe learning difficulties, mental retardation and mild heart defects in 13-year old male.
Papoulidis I, Paspaliaris V, Siomou E, Orru S, Murru R, Sifakis S, Nikolaidis P, Garas A, Sotiriou S, Thomaidis L, Manolakos E. Papoulidis I, et al. Among authors: manolakos e. Mol Cytogenet. 2015 Sep 17;8:71. doi: 10.1186/s13039-015-0175-y. eCollection 2015. Mol Cytogenet. 2015. PMID: 26388939 Free PMC article.
Prenatal detection of an inverted duplication deletion in the long arm of chromosome 1 in a fetus with increased nuchal translucency. Molecular cytogenetic analysis and review of the literature.
Manolakos E, Sifakis S, Sotiriou S, Peitsidis P, Eleftheriades M, Mersinias V, Liehr T, Thomaidis L, Kitsos G, Papoulidis I, Petersen MB, Orru S. Manolakos E, et al. Clin Dysmorphol. 2012 Apr;21(2):101-105. doi: 10.1097/MCD.0b013e32834e9279. Clin Dysmorphol. 2012. PMID: 22391621 Review. No abstract available.
103 results