Petersen MB - 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: petersen mb. 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

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: petersen mb. 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.

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

4

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: petersen mb. Prenat Diagn. 2010 Jun;30(6):586-8. doi: 10.1002/pd.2524. Prenat Diagn. 2010. PMID: 20509162 No abstract available.

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

6

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

7

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: petersen mb. 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.

8

Pure de novo partial trisomy 6p in a girl with craniosynostosis.

Varvagiannis K, Stefanidou A, Gyftodimou Y, Lord H, Williams L, Sarri C, Pandelia E, Bazopoulou-Kyrkanidou E, Noakes C, Lester T, Wilkie AO, Petersen MB. Varvagiannis K, et al. Among authors: petersen mb. Am J Med Genet A. 2013 Feb;161A(2):343-51. doi: 10.1002/ajmg.a.35727. Epub 2013 Jan 10. Am J Med Genet A. 2013. PMID: 23307468

9

First trimester diagnosis of 13q-syndrome associated with increased fetal nuchal translucency thickness. Clinical findings and systematic review.

Manolakos E, Peitsidis P, Garas A, Vetro A, Eleftheriades M, Petersen MB, Papoulidis I. Manolakos E, et al. Among authors: petersen mb. Clin Exp Obstet Gynecol. 2012;39(1):118-21. Clin Exp Obstet Gynecol. 2012. PMID: 22675970 Review.

10

Prenatal detection of an inverted duplication deletion in the long arm of chromosome 1 in a fetus with increased nuchal translucency. Molecular cytogenetic analysis and review of the literature.

Manolakos E, Sifakis S, Sotiriou S, Peitsidis P, Eleftheriades M, Mersinias V, Liehr T, Thomaidis L, Kitsos G, Papoulidis I, Petersen MB, Orru S. Manolakos E, et al. Among authors: petersen mb. Clin Dysmorphol. 2012 Apr;21(2):101-105. doi: 10.1097/MCD.0b013e32834e9279. Clin Dysmorphol. 2012. PMID: 22391621 Review. No abstract available.

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