Browsing by Author Syrrou, M.

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Showing results 40 to 46 of 46 < previous 
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Seckel syndrome in a family with three affected children and hematological manifestations associated with chromosome instabilitySyrrou, M.; Georgiou, I.; Paschopoulos, M.; Lolis, D.24-Nov-2015-
Skewed X-chromosome inactivation in Greek women with idiopathic recurrent miscarriageDasoula, A.; Kalantaridou, S.; Sotiriadis, A.; Pavlou, M.; Georgiou, I.; Paraskevaidis, E.; Makrigiannakis, A.; Syrrou, M.24-Nov-2015-
Supernumerary marker chromosomes (SMCs) in Turner syndrome are mostly derived from the Y chromosomePatsalis, P. C.; Hadjimarcou, M. I.; Velissariou, V.; Kitsiou-Tzeli, S.; Zera, C.; Syrrou, M.; Lyberatou, E.; Tsezou, A.; Galla, A.; Skordis, N.24-Nov-2015-
Unusual chromosomal mosaicism in Wolf-Hirschhorn syndrome: del(4)(p16)/der(4)(qter-q31.3::pter-qter)Syrrou, M.; Borghgraef, M.; Fryns, J. P.24-Nov-2015-
Variation in the number of FMR1 microsatellite repeats in three subgroups of the Hellenic populationSyrrou, M.; Patsalis, P. C.; Georgiou, I.; Alamanos, Y.; Pagoulatos, G.24-Nov-2015-
A watershed based segmentation method for multispectral chromosome images classificationKarvelis, P. S.; Fotiadis, D. I.; Georgiou, I.; Syrrou, M.24-Nov-2015-
Xp22.3; Yq11.2 chromosome translocation and its clinical manifestationsFrints, S. G.; Fryns, J.; Lagae, L.; Syrrou, M.; Marynen, P.; Devriendt, K.24-Nov-2015-