L. Özer

Novel Mutations in Obesity-related Genes in Turkish Children with Non-syndromic Early Onset Severe Obesity: A Multicentre Study

A. Çayır, E. Eren, A. Bideci, 2019, Journal of clinical research in pediatric endocrinology.

An Incidental Detection of a Cryptic Complex Chromosome Rearrangement Found During NGS Based PGT-SR: A Case Report

E. Unsal, S. Aktuna, A. Baltacı, 2022, Journal of Reproduction & Infertility.

Analysis of Xq27.3 Fragility Using the Micronucleus-Fluorescence In situ Hybridization Assay

H. I. Ruhi, L. Özer, I. Bökesoy, 2020, Genome integrity.

A rare cause of epileptic encephalopathy: a beta-propeller protein associated neurodegeneration case with a new mutation and literature review.

A. Yaramis, L. Özer, N. Özgün, 2020, The Turkish journal of pediatrics.

Recombinant chromosome with partial 14 q trisomy due to maternal pericentric inversion

Hande Küçük Kurtulgan, I. Sezgin, M. Yıldırım, 2015, Molecular Cytogenetics.

A novel SLC35D1 variant causing milder phenotype of Schneckenbecken dysplasia in a large pedigree

E. Unsal, V. Baltacı, L. Özer, 2022, American journal of medical genetics. Part A.

Case Report for Two Siblings Carrying Neurofibromatosis Type 1 with a Rare NF1: c.5392C>T Mutation

L. Özer, Ö. Gündüz, M. Durak, 2021, Balkan journal of medical genetics : BJMG.