E. Leze

Microdeletion and microduplication 17q21.31 plus an additional CNV, in patients with intellectual disability, identified by array-CGH.

M. Tzetis, E. Kanavakis, S. Kitsiou-Tzeli, 2012, Gene.

Milroy's primary congenital lymphedema in a male infant and review of the literature.

S. Kitsiou-Tzeli, P. Makrythanasis, C. Vrettou, 2010, In vivo.

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.

An unusual case of Cat-Eye syndrome phenotype and extragonadal mature teratoma: review of the literature.

M. Tzetis, K. Stefanaki, P. Makrythanasis, 2012, Birth defects research. Part A, Clinical and molecular teratology.

Psychomotor development of children born after preimplantation genetic diagnosis and parental stress evaluation

J. Traeger-Synodinos, E. Critselis, D. Kafetzis, 2012, World Journal of Pediatrics.

Nevoid basal carcinoma syndrome (Gorlin syndrome) and pronounced androgenic alopecia in a woman with a novel mutation p.Leu1159fsx32 in the PTCH gene

S. Kitsiou‐Tzeli, E. Kanavakis, C. Vrettou, 2011, The Journal of dermatology.

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.