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Page 1
FGFR3 related skeletal dysplasias diagnosed prenatally by ultrasonography and molecular analysis: presentation of 17 cases.
Hatzaki A, Sifakis S, Apostolopoulou D, Bouzarelou D, Konstantinidou A, Kappou D, Sideris A, Tzortzis E, Athanassiadis A, Florentin L, Theodoropoulos P, Makatsoris C, Karadimas C, Velissariou V. Hatzaki A, et al. Am J Med Genet A. 2011 Oct;155A(10):2426-35. doi: 10.1002/ajmg.a.34189. Epub 2011 Sep 9. Am J Med Genet A. 2011. PMID: 21910223
Prenatal diagnosis of hypochondroplasia: report of two cases.
Karadimas C, Sifakis S, Valsamopoulos P, Makatsoris C, Velissariou V, Nasioulas G, Petersen MB, Koumantakis E, Hatzaki A. Karadimas C, et al. Among authors: hatzaki a. Am J Med Genet A. 2006 May 1;140(9):998-1003. doi: 10.1002/ajmg.a.31177. Am J Med Genet A. 2006. PMID: 16575888
Rare XXY/XX mosaicism in a phenotypic male with Klinefelter syndrome: case report.
Velissariou V, Christopoulou S, Karadimas C, Pihos I, Kanaka-Gantenbein C, Kapranos N, Kallipolitis G, Hatzaki A. Velissariou V, et al. Among authors: hatzaki a. Eur J Med Genet. 2006 Jul-Aug;49(4):331-7. doi: 10.1016/j.ejmg.2005.09.001. Epub 2005 Oct 21. Eur J Med Genet. 2006. PMID: 16829354
Prevalence of GJB2 mutations in prelingual deafness in the Greek population.
Pampanos A, Economides J, Iliadou V, Neou P, Leotsakos P, Voyiatzis N, Eleftheriades N, Tsakanikos M, Antoniadi T, Hatzaki A, Konstantopoulou I, Yannoukakos D, Gronskov K, Brondum-Nielsen K, Grigoriadou M, Gyftodimou J, Iliades T, Skevas A, Petersen MB. Pampanos A, et al. Among authors: hatzaki a. Int J Pediatr Otorhinolaryngol. 2002 Sep 2;65(2):101-8. doi: 10.1016/s0165-5876(02)00177-5. Int J Pediatr Otorhinolaryngol. 2002. PMID: 12176179
Genetic skeletal disorders of the fetus and infant: pathologic and molecular findings in a series of 41 cases.
Konstantinidou AE, Agrogiannis G, Sifakis S, Karantanas A, Harakoglou V, Kaminopetros P, Hatzaki A, Petersen MB, Karadimas C, Velissariou V, Velonis S, Papantoniou N, Antsaklis A, Patsouris E. Konstantinidou AE, et al. Among authors: hatzaki a. Birth Defects Res A Clin Mol Teratol. 2009 Oct;85(10):811-21. doi: 10.1002/bdra.20617. Birth Defects Res A Clin Mol Teratol. 2009. PMID: 19637253
Loss of the Y chromosome PAR2 region and additional rearrangements in two familial cases of satellited Y chromosomes: cytogenetic and molecular analysis.
Velissariou V, Sismani C, Christopoulou S, Kaminopetros P, Hatzaki A, Evangelidou P, Koumbaris G, Bartsocas CS, Stylianidou G, Skordis N, Diakoumakos A, Patsalis PC. Velissariou V, et al. Among authors: hatzaki a. Eur J Med Genet. 2007 Jul-Aug;50(4):291-300. doi: 10.1016/j.ejmg.2007.04.004. Epub 2007 May 18. Eur J Med Genet. 2007. PMID: 17584536
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