Syrrou M - Search Results

1

Alpha-thalassemia intellectual disability: variable phenotypic expression among males with a recurrent nonsense mutation - c.109C>T (p.R37X).

Basehore MJ, Michaelson-Cohen R, Levy-Lahad E, Sismani C, Bird LM, Friez MJ, Walsh T, Abidi F, Holloway L, Skinner C, McGee S, Alexandrou A, Syrrou M, Patsalis PC, Raymond G, Wang T, Schwartz CE, King MC, Stevenson RE. Basehore MJ, et al. Among authors: syrrou m. Clin Genet. 2015 May;87(5):461-6. doi: 10.1111/cge.12420. Epub 2014 May 30. Clin Genet. 2015. PMID: 24805811 Review.

2

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: syrrou m. Am J Med Genet. 1999 May 28;84(3):184-90. Am J Med Genet. 1999. PMID: 10331587

3

Supernumerary marker chromosomes (SMCs) in Turner syndrome are mostly derived from the Y chromosome.

Patsalis PC, Hadjimarcou MI, Velissariou V, Kitsiou-Tzeli S, Zera C, Syrrou M, Lyberatou E, Tsezou A, Galla A, Skordis N. Patsalis PC, et al. Among authors: syrrou m. Clin Genet. 1997 Mar;51(3):184-90. doi: 10.1111/j.1399-0004.1997.tb02450.x. Clin Genet. 1997. PMID: 9137884

4

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. Am J Med Genet. 1999 May 28;84(3):306-8. Am J Med Genet. 1999. PMID: 10331614

5

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. 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

6

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. Hum Biol. 1998 Jun;70(3):621-9. Hum Biol. 1998. PMID: 9599948

7

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. 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.

8

Infertility and multiple urogenital abnormalities in a male with mosaic 46,XY/45,XO/47,XXY karyotype and mixed phenotype.

Filiadis IF, Syrrou MB, Bai MC, Georgiou IA, Pagoulatos GN, Giannakopoulos X. Filiadis IF, et al. Among authors: syrrou mb. Urol Int. 1998;61(2):111-4. doi: 10.1159/000030299. Urol Int. 1998. PMID: 9873251

9

Association of estrogen receptor gene polymorphisms with endometriosis.

Georgiou I, Syrrou M, Bouba I, Dalkalitsis N, Paschopoulos M, Navrozoglou I, Lolis D. Georgiou I, et al. Among authors: syrrou m. Fertil Steril. 1999 Jul;72(1):164-6. doi: 10.1016/s0015-0282(99)00198-3. Fertil Steril. 1999. PMID: 10428168 Free article.

10

Analysis of chromosomal aberrations in breast cancer by comparative genomic hybridization (CGH). Correlation with histoprognostic variables and c-erbB-2 immunoexpression.

Malamou-Mitsi VD, Syrrou M, Georgiou I, Pagoulatos G, Agnantis NJ. Malamou-Mitsi VD, et al. Among authors: syrrou m. J Exp Clin Cancer Res. 1999 Sep;18(3):357-61. J Exp Clin Cancer Res. 1999. PMID: 10606182

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