language Türkçe
CN

Cinkara, Neslihan

3 papers · 0 citations · 2023–2024

Publications
3
Citations
0
Years
2
Publications
Title Year Type Citations
A case of Perrault syndrome with a novel variant diagnosed at a late stage with predominance of neurological findings
EUROPEAN JOURNAL OF HUMAN GENETICS
2024 Meeting Abstract 0
A case of Perrault syndrome with a novel variant diagnosed at a late stage with predominance of neurological findings.
EUROPEAN JOURNAL OF HUMAN GENETICS
2024 Meeting Abstract 0
Novel finding in a patient with 17p13.1 deletion syndrome: a case report
EUROPEAN JOURNAL OF HUMAN GENETICS
2023 Meeting Abstract 0