Manolakos E - Search Results

1

De novo 393 kb microdeletion of 7p11.2 characterized by aCGH in a boy with psychomotor retardation and dysmorphic features.

Varvagiannis K, Papoulidis I, Koromila T, Kefalas K, Ziegler M, Liehr T, Petersen MB, Gyftodimou Y, Manolakos E. Varvagiannis K, et al. Among authors: manolakos e. Meta Gene. 2014 Apr 15;2:274-82. doi: 10.1016/j.mgene.2014.03.004. eCollection 2014 Dec. Meta Gene. 2014. PMID: 25606410 Free PMC article.

2

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. Mol Cytogenet. 2008 Nov 11;1:24. doi: 10.1186/1755-8166-1-24. Mol Cytogenet. 2008. PMID: 19014423 Free PMC article.

3

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: manolakos e. Mol Cytogenet. 2009 Jan 7;2:1. doi: 10.1186/1755-8166-2-1. Mol Cytogenet. 2009. PMID: 19128450 Free PMC article.

4

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: manolakos e. 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.

5

Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array-CGH.

Manolakos E, Vetro A, Kitmirides S, Papoulidis I, Kosyakova N, Mrasek K, Weise A, Agapitos E, Orru S, Peitsidis P, Liehr T, Petersen MB. Manolakos E, et al. Prenat Diagn. 2009 Sep;29(9):884-8. doi: 10.1002/pd.2295. Prenat Diagn. 2009. PMID: 19455597 No abstract available.

6

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. Mol Cytogenet. 2009 Dec 9;2:26. doi: 10.1186/1755-8166-2-26. Mol Cytogenet. 2009. PMID: 20003197 Free PMC article.

7

Prenatal detection of full monosomy 21 in a fetus with increased nuchal translucency: molecular cytogenetic analysis and review of the literature.

Manolakos E, Peitsidis P, Eleftheriades M, Dedoulis E, Ziegler M, Orru S, Liehr T, Petersen MB. Manolakos E, et al. J Obstet Gynaecol Res. 2010 Apr;36(2):435-40. doi: 10.1111/j.1447-0756.2009.01140.x. J Obstet Gynaecol Res. 2010. PMID: 20492403

8

A fetus with ring chromosome 21 characterized by aCGH shows no clinical findings after birth.

Papoulidis I, Manolakos E, Siomou E, Kefalas K, Thomaidis L, Liehr T, Vetro A, Athanasiadis A, Zuffardi O, Petersen MB. Papoulidis I, et al. Among authors: manolakos e. Prenat Diagn. 2010 Jun;30(6):586-8. doi: 10.1002/pd.2524. Prenat Diagn. 2010. PMID: 20509162 No abstract available.

9

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. Mol Cytogenet. 2010 Nov 9;3:22. doi: 10.1186/1755-8166-3-22. Mol Cytogenet. 2010. PMID: 21062444 Free PMC article.

10

Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boy.

Manolakos E, Sarri C, Vetro A, Kefalas K, Leze E, Sofocleus C, Kitsos G, Merou K, Kokotas H, Papadopoulou A, Attilakos A, Petersen MB, Kitsiou-Tzeli S. Manolakos E, et al. Mol Cytogenet. 2011 Feb 23;4(1):6. doi: 10.1186/1755-8166-4-6. Mol Cytogenet. 2011. PMID: 21345209 Free PMC article.

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