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You searched for: Author/Creator Balabanski, Lubomir

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1. Centenarian Exomes as a Tool for Evaluating the Clinical Relevance of Germline Tumor Suppressor Mutations. (31st March 2020)

2. Detection of pathogenic variants in Alzheimer's disease related genes in Bulgarian patients by pooled whole-exome sequencing. Issue 1 (31st December 2023)

3. Detection of pathogenic variants in Alzheimer's disease related genes in Bulgarian patients by pooled whole-exome sequencing. Issue 1 (31st December 2023)

4. Double heterozygosity of novel variants found in patients with severe clinical phenotype of cardiovascular disorders. Issue 3 (4th May 2018)

5. Genes predisposing to obesity emphasize G-protein coupled receptor associated pathways in healthy Bulgarian individuals. Issue 1 (1st January 2020)

6. Long-term follow-up of a female patient with non-classical 11β-hydroxylase deficiency and two novel mutations in CYP11B1. (2nd January 2019)

7. Novel Hypomorphic Mutation in FANCD2 Gene Observed in a Fetus with Multiple Congenital Anomalies. (23rd August 2016)

8. Prioritization of genetic variants predisposing to coronary heart disease in the Bulgarian population using centenarian exomes. Issue 1 (1st January 2019)

9. Rare genetic variants prioritize molecular pathways for semaphorin interactions in Alzheimer's disease patients. Issue 1 (1st January 2021)

10. Screening of pharmacogenetic variants associated with drug sensitivity in patients with papillary thyroid carcinoma using next generation sequencing. Issue 4 (4th July 2017)