Huri S. Aymelek
Van, Turkey
Last Updated: 09/26/2026
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Found 8 publications
Muir-Torre Syndrome with Novel Mutation in the MSH2 Gene.
Journal: Acta dermatovenerologica Croatica : ADC
Published: March 05, 2024
Autosomal recessive hypophosphatemic rickets type 2; a novel mutation in the ENPP1 gene.
Journal: The Turkish journal of pediatrics
Published: July 28, 2022
Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium.
Journal: Functional & integrative genomics
Published: July 09, 2021
Evaluation of pubertal and pathological gynaecomastia in children: A single-center experience.
Journal: Andrologia
Published: December 23, 2020
Identification of three novel pathogenic ITGA2B and one novel pathogenic ITGB3 mutations in patients with hereditary Glanzmann's thrombasthenia living in Eastern Turkey.
Journal: Platelets
Published: February 25, 2020
Genetic Burden and Outcome of Cystic Hygromas Detected Antenatally: Results of 93 Pregnancies from a Single Center in the Northern Region of Turkey.
Journal: Journal of medical ultrasound
Published: November 22, 2018
Impact of Fluorescent In Situ Hybridization Aberrations and CLLU1 Expression on the Prognosis of Chronic Lymphocytic Leukemia: Presentation of 156 Patients from Turkey.
Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology
Published: November 14, 2017
Showing 1-8 of 8
Last Updated: 09/26/2026