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CN

Cinkara, Neslihan

3 yayın · 0 atıf · 2023–2024

Yayın
3
Atıf
0
Yıllar
2
Yayınlar
Başlık Yıl Tip Atıf
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