Get started
Author

Nuray Öztürk

Observed names: N Ozturk, Nuray Ozturk
ORCID: 0000-0001-5044-0109
Observed ORCID: 0000-0001-5044-0109
OpenAlex ID: A5020936624
The clinical phenotype of Koolen‐de Vries syndrome in Turkish patients and literature review
2023 · Gokcen Karamik, Beyhan Tuysuz, et al. · American Journal of Medical Genetics Part A · 7
Clinical and molecular results in 15 Turkish patients with Wiedemann-Steiner syndrome: identification of eight novel KMT2A variants and a case of dual molecular diagnosis in the CSNK2A1
2025 · Burcu Yeter, Yasemin Kendir Demirkol, et al. · European Journal of Pediatrics · 3
Expanding the clinical and molecular features of trichorhino- phalangeal syndrome with a novel variant
2023 · Nuray Öztürk, Gökcen Karamık, et al. · The Turkish Journal of Pediatrics · 3
PDF
Genotype–phenotype correlations and functional outcomes assessed by the North Star Ambulatory Assessment in ambulatory children with dystrophinopathy
2026 · Merve Yavuz, İbrahim Bingöl, et al. · Trends in Pediatrics
PDF
Changes in bone turnover markers in adolescents with gastroesophageal reflux disease treated with lansoprazole
2022 · A Islek, N Erol Kizilelma, et al. · Acta gastro-enterologica belgica
PDF
Severe Extremity Anomaly and Neurodevelopmental Retardation in an Infant with TAR Syndrome and Differential Diagnosis in Radial Defects
2022 · Gökcen Karamık, Nuray Öztürk, et al. · The Journal of Pediatric Research
PDF
Works count: 6
Citation count: 13
H-index: 3
I10-index:
Year
Topic
Type