The significance of follow-up in patients with dysmorphic features: a case from clinical practice by Mariya Levkova, Milena Stoyanova, Mari Hachmeriyan

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Genetic counseling for hereditary cancer syndromes: a 5-year experience from a single center in Bulgaria by Mari Hachmeriyan, Mari Hachmeriyan, Mariya Levkova, Mariya Levkova, Dinnar Yahya, Dinnar Yahya, Milena Stoyanova, Milena Stoyanova, Eleonora Dimitrova

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Overview of current NGS testing for male factor infertility by Mariya Levkova, Trifon Chervenkov, Mari Hachmeriyan, Lyudmila Angelova

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Autosomal dominant macrocephaly, acquired with impaired intellectual development: a report of an ultra-rare disease by Dinnar Yahya, Milena Stoyanova, Mari Hachmeriyan, Mariya Levkova

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Diagnostic Yield of Next-Generation Sequencing for Rare Pediatric Genetic Disorders: A Single-Center Experience by Milena Stoyanova, Dinnar Yahya, Mari Hachmeriyan, Mariya Levkova

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An Ultra-Rare Disorder: Case Report on Cerebrotendinous Xanthomatosis by Mariya Levkova, Mari Hachmeriyan, Margarita Grudkova, Mihael Tsalta-Mladenov, Ara Kaprelyan

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Two Decades of Huntington’s Disease in Varna, Bulgaria: A Retrospective Single-Centre Study of Clinical Trends and Challenges by Mariya Levkova, Mihael Tsalta-Mladenov, Milena Stoyanova, Mari Hachmeriyan, Lyudmila Angelova, Ara Kaprelyan

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