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:
Mavrogiannis, LA
Argyrokastritis, A
Tzitzikas, N
Dermitzakis, E
Sarafidou, T
Patsalis, PC
Moschonas, NK
Citation: La. Mavrogiannis et al., ZNF232: structure and expression analysis of a novel human C2H2 zinc finger gene(1), member of the SCAN/LeR domain subfamily, BBA-GENE ST, 1518(3), 2001, pp. 300-305
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:
Rosser, ZH
Zerjal, T
Hurles, ME
Adojaan, M
Alavantic, D
Amorim, A
Amos, W
Armenteros, M
Arroyo, E
Barbujani, G
Beckman, G
Beckman, L
Bertranpetit, J
Bosch, E
Bradley, DG
Brede, G
Cooper, G
Corte-Real, HBSM
de Knijff, P
Decorte, R
Dubrova, YE
Evgrafov, O
Gilissen, A
Glisic, S
Golge, M
Hill, EW
Jeziorowska, A
Kalaydjieva, L
Kayser, M
Kivisild, T
Kravchenko, SA
Krumina, A
Kucinskas, V
Lavinha, J
Livshits, LA
Malaspina, P
Maria, S
McElreavey, K
Meitinger, TA
Mikelsaar, AV
Mitchell, RJ
Nafa, K
Nicholson, J
Norby, S
Pandya, A
Parik, J
Patsalis, PC
Pereira, L
Peterlin, B
Pielberg, G
Prata, ML
Previdere, C
Roewer, L
Rootsi, S
Rubinsztein, DC
Saillard, J
Santos, FR
Stefanescu, G
Sykes, BC
Tolun, A
Villems, R
Tyler-Smith, C
Jobling, MA
Citation: Zh. Rosser et al., Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language, AM J HU GEN, 67(6), 2000, pp. 1526-1543
Citation: Pc. Patsalis, FMR1 repeat analysis in patients with ovarian dysfunction or failure. (vol83, pg 329, 1999), AM J MED G, 86(3), 1999, pp. 304-304
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:
Syrrou, M
Georgiou, I
Patsalis, PC
Bouba, I
Adonakis, G
Papoulatos, GN
Citation: M. Syrrou et al., Fragile X premutations and (TA)n estrogen receptor polymorphism in women with ovarian dysfunction, AM J MED G, 84(3), 1999, pp. 306-308
Authors:
Allingham-Hawkins, SJ
Babul-Hirji, R
Chitayat, D
Holden, JJA
Yang, KT
Lee, C
Hudson, R
Gorwill, H
Nolin, SL
Glicksman, A
Jenkins, EC
Brown, WT
Howard-Peebles, PN
Becchi, C
Cummings, E
Fallon, L
Seitz, S
Black, SH
Vianna-Morgante, AM
Costa, SS
Otto, PA
Mingroni-Netto, RC
Murray, A
Webb, J
MacSwinney, F
Dennis, N
Jacobs, PA
Syrrou, M
Georgiou, I
Patsalis, PC
Uzielli, MLG
Guarducci, S
Lapi, E
Cecconi, A
Ricci, U
Citation: Sj. Allingham-hawkins et al., Fragile X premutation is a significant risk factor for premature ovarian failure: The international collaborative POF in fragile X study - Preliminary data, AM J MED G, 83(4), 1999, pp. 322-325
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
Authors:
Koptides, M
Constantinides, R
Kyriakides, G
Hadjigavriel, M
Patsalis, PC
Pierides, A
Deltas, CC
Citation: M. Koptides et al., Loss of heterozygosity in polycystic kidney disease with a missense mutation in the repeated region of PKD1, HUM GENET, 103(6), 1998, pp. 709-717