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1. Drousiotou, A; Stylianidou, G; Anastasiadou, V; Christopoulos, G; Mavrikiou, E; Georgiou, T; Kalakoutis, G; Oladimeji, A; Hara, Y; Suzuki, K; Furihata, K; Ueno, I; Ioannou, PA; Fensom, AH
   Sandhoff disease in Cyprus: population screening by biochemical and DNA analysis indicates a high frequency of carriers in the Maronite community
   HUMAN GENETICS
   
   A. Drousiotou et al., "Sandhoff disease in Cyprus: population screening by biochemical and DNA analysis indicates a high frequency of carriers in the Maronite community", HUM GENET, 107(1), 2000, pp. 12-17
2. Furihata, K; Drousiotou, A; Hara, Y; Christopoulos, G; Stylianidou, G; Anastasiadou, V; Ueno, I; Ioannou, P
   Novel splice site mutation at IVS8 nt 5 of HEXB responsible for a Greek-Cypriot case of Sandhoff disease
   HUMAN MUTATION
   
   K. Furihata et al., "Novel splice site mutation at IVS8 nt 5 of HEXB responsible for a Greek-Cypriot case of Sandhoff disease", HUM MUTAT, 13(1), 1999, pp. 38-43
3. Patsalis, PC; Sismani, C; Hettinger, JA; Boumba, I; Georgiou, I; Stylianidou, G; Anastasiadou, V; Koukoulli, R; Pagoulatos, G; Syrrou, M
   Molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes in the Hellenic population of Greece and Cyprus: Incidence, genetic variation, and stability
   AMERICAN JOURNAL OF MEDICAL GENETICS
   
   P.C. Patsalis et al., "Molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes in the Hellenic population of Greece and Cyprus: Incidence, genetic variation, and stability", AM J MED G, 84(3), 1999, pp. 184-190
4. CHRISTOPHIDOUANASTASIADOU V; SKORDIS N; STYLIANIDOU G; STANHOPE R; SPANOU E
   THE CURRY-JONES-SYNDROME - A CASE PRESENTATION
   European journal of human genetics
   
   V. Christophidouanastasiadou et al., "THE CURRY-JONES-SYNDROME - A CASE PRESENTATION", European journal of human genetics, 6, 1998, pp. 1078-1078
5. PATSALIS P; SISMANI C; HETTINGER JA; BOUMBA I; GEORGIOU I; STYLIANIDOU G; ANASTASIADOU V; KOUKOULLI R; PAGOULATOS G; SYRROU M
   POPULATION-BASED MOLECULAR SCREENING OF FRAGILE-X (FRAXA) AND FRAXE MENTAL-RETARDATION SYNDROMES - INCIDENCE, GENETIC-VARIATION AND STABILITY
   European journal of human genetics
   
   P. Patsalis et al., "POPULATION-BASED MOLECULAR SCREENING OF FRAGILE-X (FRAXA) AND FRAXE MENTAL-RETARDATION SYNDROMES - INCIDENCE, GENETIC-VARIATION AND STABILITY", European journal of human genetics, 6, 1998, pp. 4155-4155
6. ANASTASIADOU V; SYRROU M; GEORGIOU I; SISMANI C; HADJIMARCOU MI; STYLIANIDOU G; KOUKOULLI R; PATSALIS PC
   FRAXA AND FRAXE DIAGNOSIS, FREQUENCY AND MOLECULAR INVESTIGATION IN THE HELLENIC POPULATION
   Cytogenetics and cell genetics
   
   V. Anastasiadou et al., "FRAXA AND FRAXE DIAGNOSIS, FREQUENCY AND MOLECULAR INVESTIGATION IN THE HELLENIC POPULATION", Cytogenetics and cell genetics, 77(1-2), 1997, pp. 194-194
7. HARA Y; IOANNOU P; DROUSIOTOU A; STYLIANIDOU G; ANASTASIADOU V; SUZUKI K
   MUTATION ANALYSIS OF A SANDHOFF DISEASE PATIENT IN THE MARONITE COMMUNITY IN CYPRUS
   Human genetics
   
   Y. Hara et al., "MUTATION ANALYSIS OF A SANDHOFF DISEASE PATIENT IN THE MARONITE COMMUNITY IN CYPRUS", Human genetics, 94(2), 1994, pp. 136-140