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Results: 1-6 |
Results: 6

Authors: Sismani, C Al Armour, J Flint, J Girgalli, C Regan, R Patsalis, PC
Citation: C. Sismani et al., Screening for subtelomeric chromosome abnormalities in children with idiopathic mental retardation using multiprobe telomeric FISH and the new MAPH telomeric assay, EUR J HUM G, 9(7), 2001, pp. 527-532

Authors: Armour, JAL Sismani, C Patsalis, PC Cross, G
Citation: Jal. Armour et al., Measurement of locus copy number by hybridisation with amplifiable probes, NUCL ACID R, 28(2), 2000, pp. 605-609

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

Authors: Tsezou, A Hadjiathanasiou, C Gourgiotis, D Galla, A Kavazarakis, E Pasparaki, A Kapsetaki, M Sismani, C Theodoridis, C Patsalis, PC Moschonas, N Kitsiou, S
Citation: A. Tsezou et al., Molecular genetics of Turner syndrome: correlation with clinical phenotypeand response to growth hormone therapy, CLIN GENET, 56(6), 1999, pp. 441-446
Risultati: 1-6 |