Bildiri
Poster
Uluslararası
2022
Novel finding in a patient with 17p13.1 deletion syndrome: a case report
European Human Genetics Confrerence 2022
Viyana · 11.06.2022–14.06.2022 · 11.06.2022
Atıf için künye
KANJEE, M., CİNKARA, N., Yüce Kahraman, Ç., & Tatar, A. (2022). Novel finding in a patient with 17p13.1 deletion syndrome: a case report. European Human Genetics Confrerence 2022, Viyana.
BibTeX
@inproceedings{kanjee2022-233395,
author = {KANJEE, MOMEN and CİNKARA, NESLİHAN and Yüce Kahraman, Çiğdem and Tatar, Abdulgani},
title = {Novel finding in a patient with 17p13.1 deletion syndrome: a case report},
booktitle = {European Human Genetics Confrerence 2022},
address = {Viyana},
year = {2022},
url = {https://akademik.atauni.edu.tr/yayinlar/233395-novel-finding-in-a-patient-with-17p131-deletion-syndrome-a-case-report}
}