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Gökçen Karamık

Observed names: Gokcen Karamik, Gökcen Karamık
ORCID: 0000-0002-8678-1666
Observed ORCID: 0000-0002-8678-1666
OpenAlex ID: A5042613588
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
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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
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Relationship Between the Levels of 25-hydroxyvitamin D at Presentation and the Clinical, Laboratory and Follow-up Data of Children and Adolescents with Type-1 Diabetes Mellitus
2021 · Gökçen Karamık, Aslıhan Araslı Yılmaz, et al. · Journal of Academic Research in Medicine
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Works count: 5
Citation count: 13
H-index: 3
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