Authors: Skordis, N Patsalis, PC Hettinger, JA Kontou, M Herakleous, E Krishnamani, MRS Phillips, JA

Citation: N. Skordis et al., A novel arginine vasopressin-neurophysin II mutation causes autosomal dominant neurohypophyseal diabetes insipidus and morphologic pituitary changes, HORMONE RES, 53(5), 2000, pp. 239-245

Authors: Patsalis, PC Sismani, C Hettinger, JA Boumba, I Georgiou, I Stylianidou, G Anastasiadou, V Koukoulli, R Pagoulatos, G Syrrou, M

Citation: Pc. 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

Authors: Patsalis, PC Sismani, C Hettinger, JA Holden, JJA Lawson, JS Chalifoux, M Wing, M Walker, M Leggo, J

Citation: Pc. Patsalis et al., Frequencies of "grey-zone"and premutation-size FMR1 CGG-repeat alleles in patients with developmental disability in Cyprus and Canada, AM J MED G, 84(3), 1999, pp. 195-197

Authors: Patsalis, PC Sismani, C Stylianou, S Ioannou, P Joseph, G Manoli, P Holden, JJA Hettinger, JA

Citation: Pc. Patsalis et al., Genetic variation and intergenerational FMR1 CGG-repeat stability in 100 unrelated three-generation families from the normal population, AM J MED G, 84(3), 1999, pp. 217-220