20-year experience on prenatal diagnosis in a reference university medical genetics center in TurkeyBurak Durmaz, Özgür Çoğulu, Ayça Aykut et al.|TURKISH JOURNAL OF MEDICAL SCIENCES|2021Cited by 5
A novel bi-allelic variant in the SDHB gene causes a severe mitochondrial complex II deficiency: a case reportAslı Ece Solmaz, Hüseyin Önay, Erhan Parıltay et al.|Clinical Neurology and Neurosurgery|2021Cited by 2
Multipl Skleroz ve EpigenetikErhan Parıltay, Özgür Çoğulu, Aslı Ece Solmaz et al.|Unknown|2020Cited by 0
Detection of copy number variations by chromosomal microarray analysis in disorders of sex development of unexplained molecular etiology and association with clinical findingsMurat Karataş, Samim Özen, Ferda Evin et al.|Endocrine|2025Cited by 0
Identifying a rare mechanism: double parallel trisomy rescue leading to combined segmental and whole-chromosome mosaicism in an IVF-derived embryoElif Kubar, Emin Karaca, Alp Peker et al.|Journal of Assisted Reproduction and Genetics|2025Cited by 0