Kefalas K - 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: kefalas k. 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

Proximal 10q duplication in a child with severe central hypotonia characterized by array-comparative genomic hybridization: A case report and review of the literature.

Manolakos E, Vetro A, Garas A, Thomaidis L, Kefalas K, Kitsos G, Ziegler M, Liehr T, Zuffardi O, Papoulidis I. Manolakos E, et al. Among authors: kefalas k. Exp Ther Med. 2014 Apr;7(4):953-957. doi: 10.3892/etm.2014.1520. Epub 2014 Feb 6. Exp Ther Med. 2014. PMID: 24669257 Free PMC article.

3

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

4

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

5

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. Among authors: kefalas k. Mol Cytogenet. 2011 Feb 23;4(1):6. doi: 10.1186/1755-8166-4-6. Mol Cytogenet. 2011. PMID: 21345209 Free PMC article.

6

Deletion 2q31.2-q31.3 in a 4-year-old girl with microcephaly and severe mental retardation.

Manolakos E, Vetro A, Kefalas K, Thomaidis L, Aperis G, Sotiriou S, Kitsos G, Merkas M, Sifakis S, Papoulidis I, Liehr T, Zuffardi O, Petersen MB. Manolakos E, et al. Among authors: kefalas k. Am J Med Genet A. 2011 Jun;155A(6):1476-82. doi: 10.1002/ajmg.a.33981. Epub 2011 May 12. Am J Med Genet A. 2011. PMID: 21567918 No abstract available.

7

Prenatal diagnosis of two de novo 4q35-qter deletions characterized by array-CGH.

Manolakos E, Kefalas K, Vetro A, Oikonomidou E, Daskalakis G, Psara N, Siomou E, Papageorgiou E, Sevastopoulou E, Konstantinidou A, Vrachnis N, Thomaidis L, Zuffardi O, Papoulidis I. Manolakos E, et al. Among authors: kefalas k. Mol Cytogenet. 2013 Oct 31;6(1):47. doi: 10.1186/1755-8166-6-47. Mol Cytogenet. 2013. PMID: 24176130 Free PMC article.

8

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. Among authors: kefalas k. Mol Cytogenet. 2011 Apr 16;4(1):11. doi: 10.1186/1755-8166-4-11. Mol Cytogenet. 2011. PMID: 21496283 Free PMC article. No abstract available.

9

De novo 15.5-Mb Interstitial Deletion in 5p in a Male Ascertained by Oligospermia.

Papoulidis I, Vetro A, Kefalas K, Orru S, Thomaidis L, Iliodromiti Z, Zuffardi O, Manolakos E. Papoulidis I, et al. Among authors: kefalas k. Mol Syndromol. 2013 Jun;4(5):250-4. doi: 10.1159/000351656. Epub 2013 Jun 12. Mol Syndromol. 2013. PMID: 23885232 Free PMC article.

10

Partial trisomy 2p and partial monosomy 2q arising from a paternal intrachromosomal 2q-into-2p between-arm insertion and paracentric inversion: molecular cytogenetic characterization of a four-break rearrangement.

Manolakos E, Vetro A, Papadopoulou E, Kefalas K, Lagou M, Thomaidis L, Peitsidis P, Sifakis S, Divane A, Ziegler M, Liehr T, Zuffardi O, Papoulidis I. Manolakos E, et al. Among authors: kefalas k. Cytogenet Genome Res. 2013;140(1):12-20. doi: 10.1159/000350868. Epub 2013 May 4. Cytogenet Genome Res. 2013. PMID: 23652918

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

12 results

Search Page

Filters