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Browsing by Author Syrrou, M.

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Showing results 5 to 24 of 46 < previous   next >
TitleAuthor(s)Issue date???itemlist.???
Allelic imbalance of expression and epigenetic regulation within the alpha-synuclein wild-type and p.Ala53Thr alleles in Parkinson diseaseVoutsinas, G. E.; Stavrou, E. F.; Karousos, G.; Dasoula, A.; Papachatzopoulou, A.; Syrrou, M.; Verkerk, A. J.; van der Spek, P.; Patrinos, G. P.; Stoger, R.; Athanassiadou, A.24-Nov-2015-
Analysis of chromosomal aberrations in breast cancer by comparative genomic hybridization (CGH). Correlation with histoprognostic variables and c-erbB-2 immunoexpressionMalamou-Mitsi, V. D.; Syrrou, M.; Georgiou, I.; Pagoulatos, G.; Agnantis, N. J.24-Nov-2015-
Angiotensin II type 2 receptor gene polymorphism in Caucasian children with a wide spectrum of congenital anomalies of the kidney and urinary tractSiomou, E.; Bouba, I.; Kollios, K. D.; Papadopoulou, F.; Syrrou, M.; Georgiou, I.; Siamopoulou, A.24-Nov-2015-
Association of estrogen receptor gene polymorphisms with endometriosisGeorgiou, I.; Syrrou, M.; Bouba, I.; Dalkalitsis, N.; Paschopoulos, M.; Navrozoglou, I.; Lolis, D.24-Nov-2015-
Autosomal folate sensitive fragile sites in normal and mentally retarded individuals in GreeceMavrou, A.; Syrrou, M.; Tsenghi, C.; Metaxotou, C.24-Nov-2015-
A case of abetalipoproteinemia with a choreic-ataxic syndrome and none of the known mutationsKonitsiotis, S.; Mokou, C.; Kalantaridou, S.; Syrrou, M.; Kravariti, M.; Tsatoulis, A.24-Nov-2015-
A case of fetal intestinal tract distensions: prenatal biochemical and ultrasound evaluationStefos, T.; Georgiou, I.; Syrrou, M.; Lollis, D.24-Nov-2015-
Chromomycin A3-staining as an indicator of protamine deficiency and fertilizationLolis, D.; Georgiou, I.; Syrrou, M.; Zikopoulos, K.; Konstantelli, M.; Messinis, I.24-Nov-2015-
CpG methylation analysis of the MEG3 and SNRPN imprinted genes in acute myeloid leukemia and myelodysplastic syndromesBenetatos, L.; Hatzimichael, E.; Dasoula, A.; Dranitsaris, G.; Tsiara, S.; Syrrou, M.; Georgiou, I.; Bourantas, K. L.24-Nov-2015-
Dysmorphology and mental retardation: molecular cytogenetic studies in dysmorphic mentally retarded patientsVan Buggenhout, G. J.; van Ravenswaaij-Arts, C.; Mieloo, H.; Syrrou, M.; Hamel, B.; Brunner, H.; Fryns, J. P.24-Nov-2015-
Effect of Percoll gradient and swim-up preparation on the chromomycin A3 staining of normal and abnormal semen samplesGeorgiou, I.; Syrrou, M.; Stefanidis, K.; Konstantelli, M.; Lolis, D.24-Nov-2015-
Evidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and CyprusSyrrou, M.; Patsalis, P. C.; Georgiou, I.; Hadjimarcou, M. I.; Constantinou-Deltas, C. D.; Pagoulatos, G.24-Nov-2015-
Fragile X premutations and (TA)n estrogen receptor polymorphism in women with ovarian dysfunctionSyrrou, M.; Georgiou, I.; Patsalis, P. C.; Bouba, I.; Adonakis, G.; Pagoulatos, G. N.24-Nov-2015-
FRAXA and FRAXE prevalence in patients with nonspecific mental retardation in the Hellenic populationSyrrou, M.; Georgiou, I.; Grigoriadou, M.; Petersen, M. B.; Kitsiou, S.; Pagoulatos, G.; Patsalis, P. C.24-Nov-2015-
A gene for nonsyndromic X-linked mental retardation (MRX77) maps to Xq12-Xq21.33Sismani, C.; Syrrou, M.; Christodoulou, K.; Hamel, B.; Chelly, J.; Yntema, H. G.; van Bokhoven, H.; Tzoufi, M.; Georgiou, I.; Patsalis, P. C.24-Nov-2015-
Genetic and epigenetic risks of intracytoplasmic sperm injection methodGeorgiou, I.; Syrrou, M.; Pardalidis, N.; Karakitsios, K.; Mantzavinos, T.; Giotitsas, N.; Loutradis, D.; Dimitriadis, F.; Saito, M.; Miyagawa, I.; Tzoumis, P.; Sylakos, A.; Kanakas, N.; Moustakareas, T.; Baltogiannis, D.; Touloupides, S.; Giannakis, D.; Fatouros, M.; Sofikitis, N.24-Nov-2015-
Glypican 1 gene: good candidate for brachydactyly type ESyrrou, M.; Keymolen, K.; Devriendt, K.; Holvoet, M.; Thoelen, R.; Verhofstadt, K.; Fryns, J. P.24-Nov-2015-
Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene familySchlingmann, K. P.; Weber, S.; Peters, M.; Niemann Nejsum, L.; Vitzthum, H.; Klingel, K.; Kratz, M.; Haddad, E.; Ristoff, E.; Dinour, D.; Syrrou, M.; Nielsen, S.; Sassen, M.; Waldegger, S.; Seyberth, H. W.; Konrad, M.24-Nov-2015-
Increased nuchal translucency thickness in a fetus at risk for beta-thalassaemiaMakrydimas, G.; Georgiou, I.; Syrrou, M.; Skendou, C.; Lolis, D.24-Nov-2015-
Interstitial deletion of chromosome 11 (q22.3-q23.2) in a boy with mild developmental delaySyrrou, M.; Fryns, J. P.24-Nov-2015-
Showing results 5 to 24 of 46 < previous   next >