Z. Kosmaidou

Detection of numerical abnormalities of chromosome 9 and p16/CDKN2A gene alterations in ovarian cancer with fish analysis.

A. Panani, A. Rodolakis, N. Thomakos, 2012, Anticancer research.

Prenatal diagnosis of Wolf–Hirschhorn syndrome: ultrasonography and genetics

P. Antsaklis, N. Papantoniou, G. Daskalakis, 2013, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

A familial case of Muenke syndrome. Diverse expressivity of the FGFR3 Pro252Arg mutation – case report and review of the literature

C. Konialis, C. Pangalos, Christos Aravidis, 2014, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Hyperlipidemia and presence of thyroid autoantibodies in girls with Turner's syndrome or mosaic variance.

E. Deligeoroglou, D. Mitsibounas, P. Kontoleon, 1997, Journal of pediatric and adolescent gynecology.

Pregnancy in Gaucher disease.

H. Michelakakis, E. Dimitriou, S. Mesogitis, 1999, European journal of obstetrics, gynecology, and reproductive biology.

A familial case of Muenke syndrome. Diverse expressivity of the FGFR3 Pro252Arg mutation – case report and review of the literature

C. Pangalos, Christos Aravidis, Z. Kosmaidou, 2014, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.