Browsing by Author Patsalis, P. C.

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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-
Evidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and CyprusSyrrou, M.; Patsalis, P. C.; Georgiou, I.; Hadjimarcou, M. I.; Constantinou-Deltas, C. D.; Pagoulatos, G.24-Nov-2015-
FoSTeS, MMBIR and NAHR at the human proximal Xp region and the mechanisms of human Xq isochromosome formationKoumbaris, G.; Hatzisevastou-Loukidou, H.; Alexandrou, A.; Ioannides, M.; Christodoulou, C.; Fitzgerald, T.; Rajan, D.; Clayton, S.; Kitsiou-Tzeli, S.; Vermeesch, J. R.; Skordis, N.; Antoniou, P.; Kurg, A.; Georgiou, I.; Carter, N. P.; Patsalis, P. C.24-Nov-2015-
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-
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-
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-
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-