Aslıhan Sanrı
Samsun, Turkey
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 10 publications
A clinical triage score for MLPA testing in children with microcytosis suspected of deletional alpha-thalassemia.
Journal: European journal of pediatrics
Published: May 09, 2026
Clinical phenotype and long-term damage in paediatric Behçet's disease: comparative performance of ISG, ICBD and PEDBD classification criteria in a retrospective endemic cohort.
Journal: RMD open
Published: November 08, 2025
Outcomes in West syndrome: Association of genetic and perinatal etiologies with early diagnosis and therapy.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: June 01, 2025
Clinical and biochemical spectrum of APOB-related hypobetalipoproteinemia: Insights from a retrospective cohort study.
Journal: Journal of clinical lipidology
Published: October 20, 2024
Clinical and Genetic Spectrum of Myotonia Congenita in Turkish Children.
Journal: Journal of neuromuscular diseases
Published: June 25, 2023
Shared Biological Pathways and Processes in Patients with Intellectual Disability: A Multicenter Study.
Journal: Neuropediatrics
Published: February 14, 2023
Homozygous Val6Gly Variation in PRDM5 Gene Causing Brittle Cornea Syndrome: A New Turkish Case.
Journal: Molecular syndromology
Published: June 13, 2021
Comprehensive Genetic Analysis of RASopathy in the Era of Next-Generation Sequencing and Definition of a Novel Likely Pathogenic >KRAS Variation.
Journal: Molecular syndromology
Published: March 29, 2021
Targeted High-Throughput Sequencing Analysis Results of Osteogenesis Imperfecta Patients from Different Regions of Turkey.
Journal: Genetic testing and molecular biomarkers
Published: January 20, 2021
Showing 1-10 of 10
Last Updated: 09/26/2026