Orru S - 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, 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: orru s. 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.

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

3

Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridization.

Manolakos E, Kefalas K, Neroutsou R, Lagou M, Kosyakova N, Ewers E, Ziegler M, Weise A, Tsoplou P, Rapti SM, Papoulidis I, Anastasakis E, Garas A, Sotiriou S, Eleftheriades M, Peitsidis P, Malathrakis D, Thomaidis L, Kitsos G, Orru S, Liehr T, Petersen MB, Kitsiou-Tzeli S. Manolakos E, et al. Among authors: orru s. Mol Med Rep. 2010 Nov-Dec;3(6):1015-22. doi: 10.3892/mmr.2010.358. Epub 2010 Sep 10. Mol Med Rep. 2010. PMID: 21472348

4

Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome).

Manolakos E, Orru S, Neroutsou R, Kefalas K, Louizou E, Papoulidis I, Thomaidis L, Peitsidis P, Sotiriou S, Kitsos G, Tsoplou P, Petersen MB, Metaxotou A. Manolakos E, et al. Among authors: orru s. Mol Cytogenet. 2009 Dec 9;2:26. doi: 10.1186/1755-8166-2-26. Mol Cytogenet. 2009. PMID: 20003197 Free PMC article.

5

The use of array-CGH in a cohort of Greek children with developmental delay.

Manolakos E, Vetro A, Kefalas K, Rapti SM, Louizou E, Garas A, Kitsos G, Vasileiadis L, Tsoplou P, Eleftheriades M, Peitsidis P, Orru S, Liehr T, Petersen MB, Thomaidis L. Manolakos E, et al. Among authors: orru s. Mol Cytogenet. 2010 Nov 9;3:22. doi: 10.1186/1755-8166-3-22. Mol Cytogenet. 2010. PMID: 21062444 Free PMC article.

6

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: orru s. Mol Cytogenet. 2012 Feb 28;5:12. doi: 10.1186/1755-8166-5-12. Mol Cytogenet. 2012. PMID: 22373435 Free PMC article.

7

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: orru s. 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.

8

Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-CGH: Case report.

Manolakos E, Kosyakova N, Thomaidis L, Neroutsou R, Weise A, Mihalatos M, Orru S, Kokotas H, Kitsos G, Liehr T, Petersen MB. Manolakos E, et al. Among authors: orru s. Mol Cytogenet. 2008 Nov 11;1:24. doi: 10.1186/1755-8166-1-24. Mol Cytogenet. 2008. PMID: 19014423 Free PMC article.

9

Interstitial deletion at 11q14.2-11q22.1 may cause severe learning difficulties, mental retardation and mild heart defects in 13-year old male.

Papoulidis I, Paspaliaris V, Siomou E, Orru S, Murru R, Sifakis S, Nikolaidis P, Garas A, Sotiriou S, Thomaidis L, Manolakos E. Papoulidis I, et al. Among authors: orru s. Mol Cytogenet. 2015 Sep 17;8:71. doi: 10.1186/s13039-015-0175-y. eCollection 2015. Mol Cytogenet. 2015. PMID: 26388939 Free PMC article.

10

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: orru s. Cytogenet Genome Res. 2012;136(4):237-41. doi: 10.1159/000337520. Epub 2012 Apr 5. Cytogenet Genome Res. 2012. PMID: 22487875 Review.

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