Konstantinos Kefalas

发表

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

S. Kitsiou‐Tzeli, M. Petersen, A. Papadopoulou, 2011, Molecular Cytogenetics.

Non-residential real estate and economic activity: the case of Greece

I. Lekkos, P. Vlachou, Konstantinos Kefalas, 2014 .

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

T. Liehr, O. Zuffardi, S. Sifakis, 2011, American journal of medical genetics. Part A.

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

T. Liehr, Y. Gyftodimou, M. Petersen, 2014, Meta gene.

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

T. Liehr, M. Petersen, P. Peitsidis, 2010, Molecular Cytogenetics.

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

A. Konstantinidou, O. Zuffardi, A. Vetro, 2013, Molecular Cytogenetics.

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

S. Kitsiou‐Tzeli, M. Petersen, A. Papadopoulou, 2011, Molecular Cytogenetics.

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

M. Petersen, P. Peitsidis, G. Kitsos, 2009, Molecular Cytogenetics.

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

T. Liehr, O. Zuffardi, G. Kitsos, 2014, Experimental and therapeutic medicine.