1) Harry Kontos, Emmanouil Manolakos, Pantelis Malligiannis, Nicolaos Plachouras, Nikolaos Ploumis, Markos Mihalatos, Sandro Orru, Ema Anastasiadou, Michael B Petersen. Prenatal diagnosis of a fetus with 7q11.23 deletion detected by multiplex ligation-dependent probe amplification (MLPA) screening. Prenat Diagn. 2008 Jun;28(6):556-8. doi: 10.1002\/pd.2020.<\/p>\n
2) Sifakis S, Anagnostopoulou K, Plastira K, Vrachnis N, Konstantinidou A, Sklavounou E. Rare case of XX\/XY mosaicism and trisomy 13 in early prenatal diagnosis. Birth Defects Res A Clin Moleratol. 2012 Apr;94(4):245-8. Birth Defects Res A Clin Mol Teratol. 2012 Apr;94(4):245-8.<\/p>\n
3) Sarri C, Douzgou S, Kontos H, Anagnostopoulou K, T\u00fcmer Z, Grigoriadou M, Petersen MB, Kokotas H, Merou K, Pandelia E, Giouroukou E, Papanikolaou K, C\u00f4t\u00e9 GB, Gyftodimou Y. 35-Year Follow-Up of a Case of Ring Chromosome 2: Array-CGH Analysis and Literature Review of the Ring Syndrome. Cytogenet Genome Res. 2015;145(1):6-13.<\/p>\n
4) Polymeris AA, Tessa A, Anagnostopoulou K, Rubegni A, Galatolo D, Dinopoulos A, Gika AD, Youroukos S, Skouteli E, Santorelli FM, Pons R. A series of Greek children with pure hereditary pastic paraplegia: clinical features and genetic findings. J Neurol. 2016 Aug;263(8):1604-11.<\/p>\n
5) Sfontouris IA, Lainas GT, Lainas TG, Faros E, Banti M, Kardara K, Anagnostopoulou K, Kontos H, Petsas GK, Kolibianakis EM. Complex chromosomal aberrations in a fetus originating from ocytes with smooth endoplasmic reticulum (SER) aggregates. Syst Biol Reprod Med. 2018 Aug;64(4):283-290.<\/p>\n
6) Zouvelou V, Yubero D, Apostolakopoulou L, Kokkinou E, Bilanakis M, Dalivigka Z, Nikas I, Kollia E, Perez-Due\u00f1as B, Macaya A, Marc\u00e9-Grau A, Voutetakis A, Anagnostopoulou K, Kekou K, Sofocleus C, Veltra D, Kokkinis X, Fryssira H, Torres RJ, Amstrong J, Santorelli FM, Artuch R, Pons R. The genetic etiology in cerebral palsy mimics: The results from a Greek tertiary care
\ncenter. Eur J Paediatr Neurol. 2019 May;23(3):427-437.<\/p>\n
7) Benetou C, Papailiou S, Maritsi D, Anagnostopoulou K, Kontos H, Vartzelis G. A novel de noalcohol usevo KCNQ2 mutation in a child with treatment resistant
\nearly-onset epileptic encephalopathy. Turk J Pediatr. 2019;61(2):279-281.<\/p>\n","protected":false},"excerpt":{"rendered":"
1) Harry Kontos, Emmanouil Manolakos, Pantelis Malligiannis, Nicolaos Plachouras, Nikolaos Ploumis, Markos Mihalatos, Sandro Orru, Ema Anastasiadou, Michael B Petersen. Prenatal diagnosis of a fetus with 7q11.23 deletion detected by multiplex ligation-dependent probe amplification (MLPA) screening. Prenat Diagn. 2008 Jun;28(6):556-8. doi: 10.1002\/pd.2020. 2) Sifakis S, Anagnostopoulou K, Plastira K, Vrachnis N, Konstantinidou A, Sklavounou E. […]<\/p>\n","protected":false},"author":1,"featured_media":502,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"inline_featured_image":false,"footnotes":""},"categories":[36],"tags":[],"class_list":["post-1544","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-news"],"acf":[],"yoast_head":"\n