Georgiou I - Search Results

1

A gene for nonsyndromic X-linked mental retardation (MRX77) maps to Xq12-Xq21.33.

Sismani C, Syrrou M, Christodoulou K, Hamel B, Chelly J, Yntema HG, van Bokhoven H, Tzoufi M, Georgiou I, Patsalis PC. Sismani C, et al. Among authors: georgiou i. Am J Med Genet A. 2003 Sep 15;122A(1):46-50. doi: 10.1002/ajmg.a.20284. Am J Med Genet A. 2003. PMID: 12949971

2

Seckel syndrome in a family with three affected children and hematological manifestations associated with chromosome instability.

Syrrou M, Georgiou I, Paschopoulos M, Lolis D. Syrrou M, et al. Among authors: georgiou i. Genet Couns. 1995;6(1):37-41. Genet Couns. 1995. PMID: 7794560

3

Evidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and Cyprus.

Syrrou M, Patsalis PC, Georgiou I, Hadjimarcou MI, Constantinou-Deltas CD, Pagoulatos G. Syrrou M, et al. Among authors: georgiou i. Am J Med Genet. 1996 Jul 12;64(1):234-8. doi: 10.1002/(SICI)1096-8628(19960712)64:1<234::AID-AJMG42>3.0.CO;2-L. Am J Med Genet. 1996. PMID: 8826482

4

FRAXA and FRAXE prevalence in patients with nonspecific mental retardation in the Hellenic population.

Syrrou M, Georgiou I, Grigoriadou M, Petersen MB, Kitsiou S, Pagoulatos G, Patsalis PC. Syrrou M, et al. Among authors: georgiou i. Genet Epidemiol. 1998;15(1):103-9. doi: 10.1002/(SICI)1098-2272(1998)15:1<103::AID-GEPI8>3.0.CO;2-8. Genet Epidemiol. 1998. PMID: 9523214 Clinical Trial.

5

Variation in the number of FMR1 microsatellite repeats in three subgroups of the Hellenic population.

Syrrou M, Patsalis PC, Georgiou I, Alamanos Y, Pagoulatos G. Syrrou M, et al. Among authors: georgiou i. Hum Biol. 1998 Jun;70(3):621-9. Hum Biol. 1998. PMID: 9599948

6

Molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes in the Hellenic population of Greece and Cyprus: incidence, genetic variation, and stability.

Patsalis PC, Sismani C, Hettinger JA, Boumba I, Georgiou I, Stylianidou G, Anastasiadou V, Koukoulli R, Pagoulatos G, Syrrou M. Patsalis PC, et al. Among authors: georgiou i. Am J Med Genet. 1999 May 28;84(3):184-90. Am J Med Genet. 1999. PMID: 10331587

7

Fragile X premutations and (TA)n estrogen receptor polymorphism in women with ovarian dysfunction.

Syrrou M, Georgiou I, Patsalis PC, Bouba I, Adonakis G, Pagoulatos GN. Syrrou M, et al. Among authors: georgiou i. Am J Med Genet. 1999 May 28;84(3):306-8. Am J Med Genet. 1999. PMID: 10331614

8

Methylation status of the SNRPN and HUMARA genes in testicular biopsy samples.

Dasoula A, Georgiou I, Kontogianni E, Sofikitis N, Syrrou M. Dasoula A, et al. Among authors: georgiou i. Fertil Steril. 2007 Apr;87(4):805-9. doi: 10.1016/j.fertnstert.2006.09.009. Epub 2007 Jan 4. Fertil Steril. 2007. PMID: 17207798 Free article.

9

Mosaic trisomy r(14) associated with epilepsy and mental retardation.

Tzoufi M, Kanioglou C, Dasoula A, Asproudis I, Tsatsoulis A, Sismani C, Patsalis PC, Georgiou I, Syrrou M. Tzoufi M, et al. Among authors: georgiou i. J Child Neurol. 2007 Jul;22(7):869-73. doi: 10.1177/0883073807304196. J Child Neurol. 2007. PMID: 17715281

10

Skewed X-chromosome inactivation in Greek women with idiopathic recurrent miscarriage.

Dasoula A, Kalantaridou S, Sotiriadis A, Pavlou M, Georgiou I, Paraskevaidis E, Makrigiannakis A, Syrrou M. Dasoula A, et al. Among authors: georgiou i. Fetal Diagn Ther. 2008;23(3):198-203. doi: 10.1159/000116741. Epub 2008 Feb 20. Fetal Diagn Ther. 2008. PMID: 18417978

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