Aslihan Sanri
Samsun, Turkey
Last Updated: 09/26/2026
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Found 8 publications
Targeted gene panel testing in pediatric epilepsy: Diagnostic outcomes and expanding genetic insights.
Journal: Brain & development
Published: September 10, 2025
Double Genetic Diagnosis Involving MECP2 and EPHB4 in a Child with Neurodevelopmental Delay and Vascular Anomalies: A Case Report.
Journal: Molecular syndromology
Published: July 23, 2025
Diagnostic Utility of Chromosomal Microarray Analysis in a Turkish Pediatric Cohort: Insights from 1,022 Patients with Neurodevelopmental Disorders and Congenital Anomalies.
Journal: Cytogenetic and genome research
Published: May 07, 2025
Genotypic and Phenotypic Landscape of KBG Syndrome: A Study of 23 Turkish Individuals.
Journal: American journal of medical genetics. Part A
Published: April 26, 2025
YIF1B-related Kaya-Barakat-Masson Syndrome: Report of a new patient and literature review.
Journal: European journal of medical genetics
Published: November 20, 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
Cardiofaciocutaneous Syndrome Phenotype in a Case with de novo KRAS Pathogenic Variant.
Journal: Molecular syndromology
Published: October 22, 2019
Showing 1-8 of 8
Last Updated: 09/26/2026