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Items: 34

1.

10 years' experience in fragile X testing among mentally retarded individuals in Greece: a molecular and epidemiological approach.

Sofocleous C, Kitsiou S, Fryssira H, Kolialexi A, Kalaitzidaki M, Roma E, Tsangaris GT, Chistofidou C, Metaxotou C, Kanavakis E, Mavrou A.

In Vivo. 2008 Jul-Aug;22(4):451-5.

2.

Facioscapulohumeral muscular dystrophy molecular testing using a non radioactive protocol.

Kekou K, Fryssira H, Sophocleous C, Mavrou A, Manta P, Metaxotou C.

Mol Cell Probes. 2005 Dec;19(6):422-4. Epub 2005 Sep 6.

PMID:
16144755
3.

Identification of fetal nucleated red blood cells in the maternal circulation during pregnancy using anti-hemoglobin-epsilon antibody.

Mavrou A, Kolialexi A, Antsaklis A, Korantzis A, Metaxotou C.

Fetal Diagn Ther. 2003 Sep-Oct;18(5):309-13.

PMID:
12913339
4.

De novo inv(2)(p12q34) associated with Klippel-Feil anomaly and hypodontia.

Papagrigorakis MJ, Synodinos PN, Daliouris CP, Metaxotou C.

Eur J Pediatr. 2003 Sep;162(9):594-7. Epub 2003 Jun 24.

PMID:
12827510
5.

Efficiency of interphase fluorescence in situ hybridization for BCR/ABL on peripheral blood smears for monitoring of CML patients: a comparison with bone marrow findings.

Akel S, Kolialexi A, Mavrou A, Metaxotou C, Loukopoulos D, Yataganas X.

Clin Lab Haematol. 2002 Dec;24(6):361-7.

PMID:
12452817
6.

Detection of fetal NRBCs in maternal blood of pregnant carriers of beta-thalassemia using anti-gamma and anti-epsilon monoclonal antibodies.

Mavrou A, Kolialexi A, Antsaklis A, Krikos X, Koratzis A, Metaxotou C.

Ann N Y Acad Sci. 2001 Sep;945:151-2.

PMID:
11708470
7.

Use of annexin V antibody to identify apoptotic cells during pregnancy.

Kolialexi A, Tsangaris GT, Mavrou A, Antsaklis A, Tzortzatou F, Touliatou V, Metaxotou C.

Ann N Y Acad Sci. 2001 Sep;945:145-50.

PMID:
11708469
8.

Evaluation at single cell level of residual Philadelphia negative hemopoietic stem cells in chronic phase CML patients.

Akel S, Kolialexi A, Mavrou A, Metaxotou C, Loukopoulos D, Yataganas X.

Cancer Genet Cytogenet. 2000 Oct 15;122(2):93-100.

PMID:
11106818
9.

Identification of three polymorphisms in the dystrophin gene.

Kekou K, Mavrou A, Sofocleous C, Metaxotou C.

Mol Cell Probes. 1999 Dec;13(6):453-4.

PMID:
10657151
10.

Improved specificity of NRBC detection in chorionic villus sample supernatant fluids using anti-zeta and anti-epsilon monoclonal antibodies.

Mavrou A, Kolialexi A, Zheng YL, Metaxotou C, Bianchi DW.

Fetal Diagn Ther. 1999 Sep-Oct;14(5):291-5.

PMID:
10529573
11.

Cohen syndrome: two new cases in siblings.

Thomaidis L, Fryssira H, Katsarou E, Metaxotou C.

Eur J Pediatr. 1999 Oct;158(10):838-41.

PMID:
10486089
12.

Screening for minor changes in the distal part of the human dystrophin gene in Greek DMD/BMD patients.

Kekou K, Mavrou A, Florentin L, Youroukos S, Zafiriou DI, Skouteli HN, Metaxotou C.

Eur J Hum Genet. 1999 Feb-Mar;7(2):179-87.

13.

Chromosome fragility and predisposition to childhood malignancies.

Kolialexi A, Mavrou A, Tsenghi C, Tsangaris GT, Dafermou E, Tzortzatou F, Polychronopoulou S, Haidas S, Metaxotou C.

Anticancer Res. 1998 Jul-Aug;18(4A):2359-64.

PMID:
9703879
14.

Awareness and use of prenatal diagnosis among Greek women: a national survey.

Mavrou A, Metaxotou C, Trichopoulos D.

Prenat Diagn. 1998 Apr;18(4):349-55.

PMID:
9602481
15.

3' Acceptor splice site mutation in intron 50 leads to mild Duchenne muscular dystrophy phenotype.

Kekou K, Florentin L, Metaxotou C.

Hum Mutat. 1998;Suppl 1:S209-12. No abstract available.

PMID:
9452089
16.
17.

Prenatal diagnosis services in Greece.

Metaxotou C, Mavrou A, Antasaklis A.

Eur J Hum Genet. 1997;5 Suppl 1:39-41.

PMID:
9101177
18.

Mapping dystrophin gene recombinants in Greek DMD/BMD families: low recombination frequencies in the STR region.

Florentin L, Bili C, Kekou K, Tripodis N, Mavrou A, Metaxotou C.

Hum Genet. 1995 Oct;96(4):423-6.

PMID:
7557964
19.

Deletion patterns of Duchenne and Becker muscular dystrophies in Greece.

Florentin L, Mavrou A, Kekou K, Metaxotou C.

J Med Genet. 1995 Jan;32(1):48-51.

20.

Autosomal folate sensitive fragile sites in normal and mentally retarded individuals in Greece.

Mavrou A, Syrrou M, Tsenghi C, Metaxotou C.

Am J Med Genet. 1991 Feb-Mar;38(2-3):437-9.

PMID:
2018086
21.

Martin-Bell syndrome in Greece, with report of another 47,XXY fragile X patient.

Mavrou A, Syrrou M, Tsenghi C, Agelakis M, Youroukos S, Metaxotou C.

Am J Med Genet. 1988 Dec;31(4):735-9.

PMID:
3239562
22.

Prenatal diagnosis of chromosomal abnormalities from chorionic biopsy samples: improved success rate using a modified direct method.

Metaxotou C, Antsaklis A, Panagiotopoulou P, Benetou M, Mavrou A, Matsaniotis N.

Prenat Diagn. 1987 Sep;7(7):461-9.

PMID:
3671333
23.

Evidence for reduced recombination on the nondisjoined chromosomes 21 in Down syndrome.

Warren AC, Chakravarti A, Wong C, Slaugenhaupt SA, Halloran SL, Watkins PC, Metaxotou C, Antonarakis SE.

Science. 1987 Aug 7;237(4815):652-4.

PMID:
2955519
24.

Reduced recombination rate on chromosomes 21 that have undergone nondisjunction.

Antonarakis SE, Chakravarti A, Warren AC, Slaugenhaupt SA, Wong C, Halloran SL, Metaxotou C.

Cold Spring Harb Symp Quant Biol. 1986;51 Pt 1:185-90. No abstract available.

PMID:
3034482
25.

Analysis of DNA haplotypes suggests a genetic predisposition to trisomy 21 associated with DNA sequences on chromosome 21.

Antonarakis SE, Kittur SD, Metaxotou C, Watkins PC, Patel AS.

Proc Natl Acad Sci U S A. 1985 May;82(10):3360-4.

26.

Linkage map on chromosome 21q and the association of a DNA haplotype with a propensity to nondisjunction and trisomy 21.

Antonarakis SE, Kittur SD, Metaxotou C, Bartsocas C, Kitsiou S, Watkins PC, Patel AS, Warren AC, Gusella JF, Groner Y, et al.

Ann N Y Acad Sci. 1985;450:95-107. No abstract available.

PMID:
2990311
27.

A familial X/Y translocation in a boy with ichthyosis, hypogonadism and mental retardation.

Metaxotou C, Ikkos D, Panagiotopoulou P, Alevizaki M, Mavrou A, Tsenghi C, Matsaniotis N.

Clin Genet. 1983 Nov;24(5):380-3.

PMID:
6652948
28.

Fetal karyotypes from fetoscopy blood samples.

Metaxotou C, Antsaklis A, Panagiotopoulou P, Tsenghi C, Benetou M, Mavrou A, Matsaniotis N.

Prenat Diagn. 1983 Apr-Jun;3(2):173-5.

PMID:
6578501
29.

Parental chromosome translocations and fetal loss.

Tsenghi C, Metaxotou C, Kalpini-Mavrou A, Strataki-Benetou M, Matsaniotis N.

Obstet Gynecol. 1981 Oct;58(4):456-8.

PMID:
7279340
30.

Trisomy 3 mosaicism in a live-born infant.

Metaxotou C, Tsenghi C, Bitzos I, Strataki-Benetou M, Kalpini-Mavrou A, Matsaniotis N.

Clin Genet. 1981 Jan;19(1):37-40.

PMID:
7460379
31.

A de novo interstitial deletion of band q21 on chromosome 6.

Cote GB, Papadakou-Lagoyanni S, Metaxotou C.

Ann Genet. 1981;24(3):170-1. No abstract available.

PMID:
6974529
32.

Polymorphism of chromosome 9 in 600 Greek subjects.

Metaxotou C, Kalpini-Mavrou A, Panagou M, Tsenghi C.

Am J Hum Genet. 1978 Jan;30(1):85-9.

33.

Ring chromosome 9. 46,XY,r(9) in a male with ambiguous external genitalia.

Metaxotou C, Kalpini-Mavrou A.

Hum Genet. 1977 Jul 26;37(3):351-4.

PMID:
885556
34.

The "D" syndrome. Report of four trisomic and one D/D translocation case.

Conen PE, Erkman B, Metaxotou C.

Am J Dis Child. 1966 Mar;111(3):236-47. No abstract available.

PMID:
4221938

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