Serkan Kabacam
Ankara, Turkey
Last Updated: 09/26/2026
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Found 8 publications
Investigation of the genetic background of familial hypercholesterolemia in a Turkish cohort and its clinical implications.
Journal: Journal of clinical lipidology
Published: September 22, 2024
Genetic IGF1R defects: new cases expand the spectrum of clinical features.
Journal: Journal of endocrinological investigation
Published: January 31, 2020
A novel mutation of keratin 5 in epidermolysis bullosa simplex with migratory circinate erythema.
Journal: Pediatric dermatology
Published: January 23, 2020
Clock gene PERIOD3 polymorphism is associated with susceptibility to Graves' disease but not to Hashimoto's thyroiditis.
Journal: Chronobiology international
Published: July 23, 2019
Clinical and molecular evaluation of 16 patients with Rett syndrome.
Journal: The Turkish journal of pediatrics
Published: August 14, 2018
Epigenotype and phenotype correlations in patients with Beckwith-Wiedemann syndrome.
Journal: The Turkish journal of pediatrics
Published: January 01, 2018
A novel missense mutation of the GRK1 gene in Oguchi disease.
Journal: Molecular medicine reports
Published: March 06, 2016
Showing 1-8 of 8
Last Updated: 09/26/2026