Zaránd Némethi

Clinical evaluation of rare copy number variations identified by chromosomal microarray in a Hungarian neurodevelopmental disorder patient cohort

G. Fekete, Anna Lengyel, I. Haltrich, 2022, Molecular Cytogenetics.

Enhancing Molecular Testing for Effective Delivery of Actionable Gene Diagnostics

G. Fekete, Á. Kovács, Tünde Abonyi, 2022, Bioengineering.