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Browsing by Author Syrrou, M.

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Showing results 17 to 36 of 46 < previous   next >
TitleAuthor(s)Issue date???itemlist.???
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-
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-
Showing results 17 to 36 of 46 < previous   next >