Browsing by Author Syrrou, M.

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Showing results 36 to 46 of 46 < previous 
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Refining the locus of branchio-otic syndrome 2 (BOS2) to a 5.25 Mb locus on chromosome 1q31.3q32.1Thienpont, B.; Dimitriadou, E.; Theodoropoulos, K.; Breckpot, J.; Fryssira, H.; Kitsiou-Tzeli, S.; Tzoufi, M.; Vermeesch, J. R.; Syrrou, M.; Devriendt, K.24-Nov-2015-
Refractory photosensitive epilepsy associated with a complex rearrangement of chromosome 2Van Esch, H.; Syrrou, M.; Lagae, L.24-Nov-2015-
Retrotransposon RNA expression and evidence for retrotransposition events in human oocytesGeorgiou, I.; Noutsopoulos, D.; Dimitriadou, E.; Markopoulos, G.; Apergi, A.; Lazaros, L.; Vaxevanoglou, T.; Pantos, K.; Syrrou, M.; Tzavaras, T.24-Nov-2015-
The role of stress in female reproduction and pregnancy: an updateVrekoussis, T.; Kalantaridou, S. N.; Mastorakos, G.; Zoumakis, E.; Makrigiannakis, A.; Syrrou, M.; Lavasidis, L. G.; Relakis, K.; Chrousos, G. P.24-Nov-2015-
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-