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Journal of Clinical Medicine|August 28, 2025
Genomic Evaluation of AML-Main Techniques and Novel ApproachesDinnar Yahya, Milena Stoyanova, Mari Hachmeriyan, et al.Medical Sciences (Basel, Switzerland)|January 23, 2025
NIPT Integration as a Patient-Paid Prenatal Screening Option-Observations and Challenges from a Bulgarian Genetic Counseling CenterDinnar Yahya, Mari Hachmeriyan, Milena Stoyanova, et al.Medical Sciences (Basel, Switzerland)|June 25, 2025
Diagnostic Yield of Next-Generation Sequencing for Rare Pediatric Genetic Disorders: A Single-Center ExperienceMilena Stoyanova, Dinnar Yahya, Mari Hachmeriyan, et al.Journal of the American Association of Nurse Practitioners|May 4, 2023
Congenital myasthenic syndrome due to a genetic mutationMihael Tsalta-Mladenov, Mariya Levkova, Darina Georgieva, et al.Folia Medica|March 2, 2021
16p11.2 Duplication Syndrome - a Case ReportMariya Levkova, Milena Stoyanova, Rada Staneva, et al.Romanian Journal of Internal Medicine = Revue Roumaine De Medecine Interne|August 31, 2019
Comparison between thrombophilic gene polymorphisms among high risk patientsMariya Levkova, Mari Hachmeriyan, Milena Stoyanova, et al.Oncology Reviews|August 11, 2025
Genetic counseling for hereditary cancer syndromes: a 5-year experience from a single center in BulgariaMari Hachmeriyan, Mariya Levkova, Dinnar Yahya, et al.Healthcare (Basel, Switzerland)|April 26, 2025
Ethical and Psychosocial Issues Associated with Genetic Testing for Hereditary Tumor Predisposition SyndromesMari Hachmeriyan, Mariya Levkova, Dinnar Yahya, et al.Reports (MDPI)|July 25, 2025
An Ultra-Rare Disorder: Case Report on Cerebrotendinous XanthomatosisMariya Levkova, Mari Hachmeriyan, Margarita Grudkova, et al.Journal of the American Association of Nurse Practitioners|June 22, 2022
Variants of uncertain significance in the era of next-generation sequencingMariya Levkova, Milena Stoyanova, Miroslava Benkova-Petrova, et al.Pageof 3