Kontodiou M - Search Results

1

Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male.

Kitsiou-Tzeli S, Manolakos E, Lagou M, Kontodiou M, Kosyakova N, Ewers E, Weise A, Garas A, Orru S, Liehr T, Metaxotou A. Kitsiou-Tzeli S, et al. Among authors: kontodiou m. Mol Cytogenet. 2009 Jan 7;2:1. doi: 10.1186/1755-8166-2-1. Mol Cytogenet. 2009. PMID: 19128450 Free PMC article.

2

Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male.

Kitsiou-Tzeli S, Manolakos E, Lagou M, Anagnostopoulou K, Kontodiou M, Kosyakova N, Ewers E, Weise A, Garas A, Orru S, Liehr T, Metaxotou A. Kitsiou-Tzeli S, et al. Among authors: kontodiou m. Mol Cytogenet. 2009 Feb 20;2:8. doi: 10.1186/1755-8166-2-8. Mol Cytogenet. 2009. PMID: 19232114 Free PMC article. No abstract available.

3

Prenatal diagnosis of Wolf-Hirschhorn syndrome confirmed by comparative genomic hybridization array: report of two cases and review of the literature.

Sifakis S, Manolakos E, Vetro A, Kappou D, Peitsidis P, Kontodiou M, Garas A, Vrachnis N, Konstandinidou A, Zuffardi O, Orru S, Papoulidis I. Sifakis S, et al. Among authors: kontodiou m. Mol Cytogenet. 2012 Feb 28;5:12. doi: 10.1186/1755-8166-5-12. Mol Cytogenet. 2012. PMID: 22373435 Free PMC article.

4

A de novo 2.9 Mb interstitial deletion at 13q12.11 in a child with developmental delay accompanied by mild dysmorphic characteristics.

Lagou M, Papoulidis I, Orru S, Papadopoulos V, Daskalakis G, Kontodiou M, Anastasakis E, Petersen MB, Kitsos G, Thomaidis L, Manolakos E. Lagou M, et al. Among authors: kontodiou m. Mol Cytogenet. 2014 Dec 3;7(1):92. doi: 10.1186/s13039-014-0092-5. eCollection 2014. Mol Cytogenet. 2014. PMID: 25506395 Free PMC article.

5

Tetrasomy 9p mosaicism associated with a normal phenotype in two cases.

Papoulidis I, Kontodiou M, Tzimina M, Saitis I, Hamid AB, Klein E, Kosyakova N, Kordass U, Kunz J, Siomou E, Nicolaides P, Orru S, Thomaidis L, Liehr T, Petersen MB, Manolakos E. Papoulidis I, et al. Among authors: kontodiou m. Cytogenet Genome Res. 2012;136(4):237-41. doi: 10.1159/000337520. Epub 2012 Apr 5. Cytogenet Genome Res. 2012. PMID: 22487875 Free article. Review.

6

Prenatal detection of TAR syndrome in a fetus with compound inheritance of an RBM8A SNP and a 334‑kb deletion: a case report.

Papoulidis I, Oikonomidou E, Orru S, Siomou E, Kontodiou M, Eleftheriades M, Bacoulas V, Cigudosa JC, Suela J, Thomaidis L, Manolakos E. Papoulidis I, et al. Among authors: kontodiou m. Mol Med Rep. 2014 Jan;9(1):163-5. doi: 10.3892/mmr.2013.1788. Epub 2013 Nov 11. Mol Med Rep. 2014. PMID: 24220582

7

Complex Rearrangement Involving Three Chromosomes, Four Breakpoints and a 2.7-Mb Deletion in the 18q Segment Observed in a Girl with Mild Learning Difficulties.

Kontodiou M, Daskalakis G, Vetro A, Paspaliaris V, Papaioannou G, Dagklis T, Tsakiridis I, Ziegler M, Liehr T, Thomaidis L, Papoulidis I, Manolakos E. Kontodiou M, et al. Cytogenet Genome Res. 2015;147(2-3):118-23. doi: 10.1159/000442583. Epub 2015 Dec 18. Cytogenet Genome Res. 2015. PMID: 26681178

8

Dual testing with QF-PCR and karyotype analysis for prenatal diagnosis of chromosomal abnormalities. Evaluation of 13,500 cases with consideration of using QF-PCR as a stand-alone test according to referral indications.

Papoulidis I, Siomou E, Sotiriadis A, Efstathiou G, Psara A, Sevastopoulou E, Anastasakis E, Sifakis S, Tsiligianni T, Kontodiou M, Malamaki C, Tzimina M, Petersen MB, Manolakos E, Athanasiadis A. Papoulidis I, et al. Among authors: kontodiou m. Prenat Diagn. 2012 Jul;32(7):680-5. doi: 10.1002/pd.3888. Epub 2012 Apr 18. Prenat Diagn. 2012. PMID: 22513450

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