A DE NOVO INTERSTITIAL DELETION OF BAND Q21 ON CHROMOSOME 6COTE GB; PAPADAKOU LAGOYANNI S; METAXOTOU C et al.1981; ANN. GENET.; FRA; DA. 1981; VOL. 24; NO 3; PP. 170-171; ABS. FRE; BIBL. 2 REF.Article

POLYMORPHISM OF CHROMOSOME 9 IN 600 GREEK SUBJECTS.METAXOTOU C; KALPINI MAVROU A; PANAGOU M et al.1977; AMER. J. HUM. GENET.; U.S.A.; DA. 1977; VOL. 30; NO 1; PP. 85-89; BIBL. 13 REF.Article

Cohen syndrome : two new cases in siblingsTHOMAIDIS, L; FRYSSIRA, H; KATSAROU, E et al.European journal of pediatrics. 1999, Vol 158, Num 10, pp 838-841, issn 0340-6199Article

Awareness and use of prenatal diagnosis among greek women : A national surveyMAVROU, A; METAXOTOU, C; TRICHOPOULOS, D et al.Prenatal diagnosis. 1998, Vol 18, Num 4, pp 349-355, issn 0197-3851Article

Autosomal folate sensitive fragile sites in normal and mentally retarded individuals in GreeceMAVROU, A; SYRROU, M; TSENGHI, C et al.American journal of medical genetics. 1991, Vol 38, Num 2-3, pp 437-439, issn 0148-7299Article

PARENTAL CHROMOSOME TRANSLOCATIONS AND FETAL LOSSTSENGHI C; METAXOTOU C; KALPINI MAVROU A et al.1981; OBSTET. GYNECOL. (N. Y., 1953); ISSN 0029-7844; USA; DA. 1981; VOL. 58; NO 4; PP. 456-458; BIBL. 8 REF.Article

Identification of fetal nucleated red blood cells in the maternal circulation during pregnancy using anti-hemoglobin-ε antibodyMAVROU, A; KOLIALEXI, A; ANTSAKLIS, A et al.Fetal diagnosis and therapy. 2003, Vol 18, Num 5, pp 309-313, issn 1015-3837, 5 p.Article

Improved specificity of NRBC detection in chorionic villus sample supernatant fluids using anti-zeta and anti-epsilon monoclonal antibodiesMAVROU, A; KOLIALEXI, A; ZHENG, Y.-L et al.Fetal diagnosis and therapy. 1999, Vol 14, Num 5, pp 291-295, issn 1015-3837Conference Paper

Analysis of DNA haplotypes suggests a genetic predisposition to trisomy 21 associated with DNA sequences on chromosome 21ANTONARAKIS, S. E; KITTUR, S. D; METAXOTOU, C et al.Proceedings of the National Academy of Sciences of the United States of America. 1985, Vol 82, Num 10, pp 3360-3364, issn 0027-8424Article

Fetal nucleated erythrocytes (NRBCS) in chorionic villus sample supernatant fluids: An additional source of fetal material for karyotype confirmationMAVROU, A; ZHENG, Y.-L; KOLIALEXI, A et al.Prenatal diagnosis. 1997, Vol 17, Num 7, pp 643-649, issn 0197-3851Article

Martin-Bell syndrome in Greece, with report of another 47,XXY fragile X patientMAVROU, A; SYRROU, M; TSENGHI, C et al.American journal of medical genetics. 1988, Vol 31, Num 4, pp 735-739, issn 0148-7299Article

Evidence for reduced recombination on the nondisjoined chromosomes 21 in down syndromeWARREN, A. C; ARAVINDA CHAKRAVARTI; WONG, C et al.Science (Washington, D.C.). 1987, Vol 237, Num 4815, pp 652-654, issn 0036-8075Article

The meiotic stage of nondisjunction in trisomy 21 : determination by using DNA polymorphismsANTONARAKIS, S. E; PETERSEN, M. B; COHEN, M. M et al.American journal of human genetics. 1992, Vol 50, Num 3, pp 544-550, issn 0002-9297Article