EP
Ercoskun, Pelin
8 yayın · 29 atıf · 2021–2024
Yayın
8
Atıf
29
Yıllar
4
Yayınlar
| Başlık | Yıl | Tip | Atıf |
|---|---|---|---|
|
Whole Exome Sequencing in Neurodevelopmental Disorders: A Single Center Study
|
2024 | Article | 0 |
|
The right to terminate pregnancy (abortion): reflections from Turkey
|
2023 | Article | 1 |
|
Genetic Characterization of Hereditary Cancer Syndromes Based on Targeted Next-Generation Sequencing
|
2022 | Article | 7 |
|
A new case of Turnpenny-Fry syndrome
|
2022 | Article | 5 |
|
A Novel nonsense variant in the <i>CDH2</i> gene associated with ACOGS: A case report
|
2022 | Article | 5 |
|
A novel genomic variant in two siblings with very low-density lipoprotein receptor-associated cerebellar hypoplasia
|
2022 | Article | 0 |
|
Novel Findings in Floating-Harbor Syndrome and a Mini-Review of the Literature
|
2021 | Article | 6 |
|
Witteveen-Kolk syndrome: The first patient from Turkey
|
2021 | Article | 5 |