A. Xaidara

De novo interstitial duplication of the 15q11.2‐q14 PWS/AS region of maternal origin: Clinical description, array CGH analysis, and review of the literature

M. Tzetis, E. Kanavakis, S. Kitsiou-Tzeli, 2010, American journal of medical genetics. Part A.

A boy with conduct disorder (CD), attention deficit hyperactivity disorder (ADHD), borderline intellectual disability, and 47,XXY syndrome in combination with a 7q11.23 duplication, 11p15.5 deletion, and 20q13.33 deletion

M. Tzetis, G. Kolaitis, S. Kitsiou-Tzeli, 2016, Child and Adolescent Psychiatry and Mental Health.

The clinical utility of molecular karyotyping using high-resolution array-comparative genomic hybridization

S. Kitsiou‐Tzeli, M. Tzetis, E. Kanavakis, 2012, Expert review of molecular diagnostics.

Microduplication 3q13.2q13.31 identified in a male with dysmorphic features and multiple congenital anomalies

S. Kitsiou‐Tzeli, M. Tzetis, E. Kanavakis, 2014, American journal of medical genetics. Part A.