Browsing by Author Syrrou, M.

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Jump to: Α Β Γ Δ Ε Ζ Η Θ Ι Κ Λ Μ Ν Ξ Ο Π Ρ Σ Τ Υ Φ Χ Ψ Ω
or enter first few letters:  
View Option
Showing results 25 to 44 of 46 < previous   next >
TitleAuthor(s)Issue date???itemlist.???
Kennedy disease: avoiding misdiagnosisPaparounas, K.; Gotsi, A.; Syrrou, M.; Akritidis, N.24-Nov-2015-
Lack of association of birth size with polymorphisms of two imprinted genes, IGF2R and GRB10Kukuvitis, A.; Georgiou, I.; Syrrou, M.; Andronikou, S.; Dickerman, Z.; Islam, A.; McCann, J.; Polychronakos, C.24-Nov-2015-
Martin-Bell syndrome in Greece, with report of another 47,XXY fragile X patientMavrou, A.; Syrrou, M.; Tsenghi, C.; Agelakis, M.; Youroukos, S.; Metaxotou, C.24-Nov-2015-
Methylation status of the SNRPN and HUMARA genes in testicular biopsy samplesDasoula, A.; Georgiou, I.; Kontogianni, E.; Sofikitis, N.; Syrrou, M.24-Nov-2015-
Molecular cytogenetic characterization and origin of two de novo duplication 9p casesTsezou, A.; Kitsiou, S.; Galla, A.; Petersen, M. B.; Karadima, G.; Syrrou, M.; Sahlen, S.; Blennow, E.24-Nov-2015-
Molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes in the Hellenic population of Greece and Cyprus: incidence, genetic variation, and stabilityPatsalis, P. C.; Sismani, C.; Hettinger, J. A.; Boumba, I.; Georgiou, I.; Stylianidou, G.; Anastasiadou, V.; Koukoulli, R.; Pagoulatos, G.; Syrrou, M.24-Nov-2015-
Mosaic trisomy r(14) associated with epilepsy and mental retardationTzoufi, M.; Kanioglou, C.; Dasoula, A.; Asproudis, I.; Tsatsoulis, A.; Sismani, C.; Patsalis, P. C.; Georgiou, I.; Syrrou, M.24-Nov-2015-
Mosaicism for duplication 12q (12q13-->12q21.2) accompanied by a pericentric inversion in a dysmorphic female infantVermeesch, J. R.; Syrrou, M.; Salden, I.; Dhondt, F.; Matthijs, G.; Fryns, J. P.24-Nov-2015-
Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemiaSchlingmann, K. P.; Sassen, M. C.; Weber, S.; Pechmann, U.; Kusch, K.; Pelken, L.; Lotan, D.; Syrrou, M.; Prebble, J. J.; Cole, D. E.; Metzger, D. L.; Rahman, S.; Tajima, T.; Shu, S. G.; Waldegger, S.; Seyberth, H. W.; Konrad, M.24-Nov-2015-
Oestrogen receptor gene polymorphisms and ovarian stimulation for in-vitro fertilizationGeorgiou, I.; Konstantelli, M.; Syrrou, M.; Messinis, I. E.; Lolis, D. E.24-Nov-2015-
Promoter hypermethylation of the MEG3 (DLK1/MEG3) imprinted gene in multiple myelomaBenetatos, L.; Dasoula, A.; Hatzimichael, E.; Georgiou, I.; Syrrou, M.; Bourantas, K. L.24-Nov-2015-
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-