Syrrou M - Search Results

1

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.

2

Oestrogen receptor gene polymorphisms and ovarian stimulation for in-vitro fertilization.

Georgiou I, Konstantelli M, Syrrou M, Messinis IE, Lolis DE. Georgiou I, et al. Among authors: syrrou m. Hum Reprod. 1997 Jul;12(7):1430-3. doi: 10.1093/humrep/12.7.1430. Hum Reprod. 1997. PMID: 9262271

3

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

4

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

5

Increased nuchal translucency thickness in a fetus at risk for beta-thalassaemia.

Makrydimas G, Georgiou I, Syrrou M, Skendou C, Lolis D. Makrydimas G, et al. Among authors: syrrou m. J Matern Fetal Med. 1997 Sep-Oct;6(5):301-2. doi: 10.1002/(SICI)1520-6661(199709/10)6:5<301::AID-MFM13>3.0.CO;2-N. J Matern Fetal Med. 1997. PMID: 9360192

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

Effect of Percoll gradient and swim-up preparation on the chromomycin A3 staining of normal and abnormal semen samples.

Georgiou I, Syrrou M, Stefanidis K, Konstantelli M, Lolis D. Georgiou I, et al. Among authors: syrrou m. Andrologia. 1998 Mar-Apr;30(2):101-4. doi: 10.1111/j.1439-0272.1998.tb01154.x. Andrologia. 1998. PMID: 9629431

8

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. Genet Couns. 1995;6(1):37-41. Genet Couns. 1995. PMID: 7794560

9

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

10

Chromomycin A3-staining as an indicator of protamine deficiency and fertilization.

Lolis D, Georgiou I, Syrrou M, Zikopoulos K, Konstantelli M, Messinis I. Lolis D, et al. Among authors: syrrou m. Int J Androl. 1996 Feb;19(1):23-7. doi: 10.1111/j.1365-2605.1996.tb00429.x. Int J Androl. 1996. PMID: 8698534

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