language English
KM

Kanjee, Momen

7 yayın · 10 atıf · 2022–2024

Yayın
7
Atıf
10
Yıllar
3
Yayınlar
Başlık Yıl Tip Atıf
A decade of insights: prenatal cytogenetic diagnosis results of high-risk pregnancies at Ataturk University Medical Genetics laboratory (ATAGEN)
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
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
Whole Exome Sequencing in Neurodevelopmental Disorders: A Single Center Study
BASIC AND CLINICAL NEUROSCIENCE
2024 Article 0
Novel finding in a patient with 17p13.1 deletion syndrome: a case report
EUROPEAN JOURNAL OF HUMAN GENETICS
2023 Meeting Abstract 0
A new case of Turnpenny-Fry syndrome
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
2022 Article 5
A Novel nonsense variant in the <i>CDH2</i> gene associated with ACOGS: A case report
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
2022 Article 5