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Repository of UOI "Olympias"
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Browsing by Author Syrrou, M.
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Showing results 17 to 36 of 46
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Fragile X premutations and (TA)n estrogen receptor polymorphism in women with ovarian dysfunction
Syrrou, 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 population
Syrrou, 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-Xq21.33
Sismani, 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 method
Georgiou, 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 E
Syrrou, 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 family
Schlingmann, 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-thalassaemia
Makrydimas, 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 delay
Syrrou, M.
;
Fryns, J. P.
24-Nov-2015
-
Kennedy disease: avoiding misdiagnosis
Paparounas, K.
;
Gotsi, A.
;
Syrrou, M.
;
Akritidis, N.
24-Nov-2015
-
Lack of association of birth size with polymorphisms of two imprinted genes, IGF2R and GRB10
Kukuvitis, 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 patient
Mavrou, 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 samples
Dasoula, A.
;
Georgiou, I.
;
Kontogianni, E.
;
Sofikitis, N.
;
Syrrou, M.
24-Nov-2015
-
Molecular cytogenetic characterization and origin of two de novo duplication 9p cases
Tsezou, 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 stability
Patsalis, 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 retardation
Tzoufi, 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 infant
Vermeesch, 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 hypocalcemia
Schlingmann, 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 fertilization
Georgiou, 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 myeloma
Benetatos, 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 1q31.3q32.1
Thienpont, B.
;
Dimitriadou, E.
;
Theodoropoulos, K.
;
Breckpot, J.
;
Fryssira, H.
;
Kitsiou-Tzeli, S.
;
Tzoufi, M.
;
Vermeesch, J. R.
;
Syrrou, M.
;
Devriendt, K.
24-Nov-2015
-