SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler
Brittle cornea syndrome with a novel pathogenic variant of PRDM5 gene
EUROPEAN JOURNAL OF HUMAN GENETICS
, cilt.30, sa.SUPPL 1, ss.119-120, 2022 (SCI-Expanded)
Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar
Rekombinant Kromozom 8 Sendromlu Nadir Bir Prenatal Olgu
15. Ulusal Tıbbi Genetik Kongresi, Muğla, Türkiye, 9 - 13 Kasım 2022, ss.90
A Novel Mutation of DYSF Gene in A Patient with Limb Girdle Muscular Dystrophy Type 2b
European Human Genetics Virtual Conference, 06 Haziran 2020
MACROORCHIDISM AS A UNIQUE SIGN IN 3q13.31 DELETION SYNDROME
ESHG 2019, Gothenburg, İsveç, 15 - 19 Haziran 2019, cilt.27, ss.1843
Macroorchidism as a Uniq Sign in 3q13.31 Deletion Syndrome.
European Human Genetics Conference, Gothenburg, İsveç, 15 Haziran 2019, cilt.27, ss.1843
A Patient with a Balanced Inversion of Chromosome 11 and Unbalancded Inversion of Chromosome 2.
Erciyes Medical Genetics Days, Kayseri, Türkiye, 21 Şubat 2019, cilt.21, ss.20