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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.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.Children (Basel, Switzerland)|May 4, 2026
Diagnostic Yield and Genotype-Phenotype Overlap in Pediatric Autism Spectrum Disorder Patients Using Whole-Exome Sequencing and Phenotype-Driven Variant Interpretation: A Single-Center Cohort StudyAndreya Yaneva, Mariya Levkova, Milena Stoyanova, et al.Neurology International|June 25, 2025
Two Decades of Huntington's Disease in Varna, Bulgaria: A Retrospective Single-Centre Study of Clinical Trends and ChallengesMariya Levkova, Mihael Tsalta-Mladenov, Milena Stoyanova, et al.Folia Medica|July 19, 2022
Molecular screening for fragile X syndrome in children with unexplained intellectual disability and/or autistic behaviourMilena Stoyanova, Mari Hachmeriyan, Mariya Levkova, et al.Behaviour Research and Therapy|October 31, 2006
Cognitive behavioral therapy for panic disorder and comorbidity: more of the same or less of more?Michelle G Craske, Todd J Farchione, Laura B Allen, et al.European Journal of Human Genetics : EJHG|October 21, 2020
The clinical significance of A2ML1 variants in Noonan syndrome has to be reconsideredJulia Brinkmann, Christina Lissewski, Valentina Pinna, et al.Pageof 2