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Browsing by Author Sismani, C.

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Showing results 1 to 4 of 4
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Clinical application of whole-genome array CGH during prenatal diagnosis: Study of 25 selected pregnancies with abnormal ultrasound findings or apparently balanced structural aberrationsEvangelidou, P.; Sismani, C.; Ioannides, M.; Christodoulou, C.; Koumbaris, G.; Kallikas, I.; Georgiou, I.; Velissariou, V.; 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-
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-
Showing results 1 to 4 of 4