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- Clinical utilities and end-user experience of pharmacogenomics: 39 mo of clinical implementation experience in an Australian hospital setting
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- Role of IL-2/IL-2 receptor in pathogenesis of autoimmune disorders: Genetic and therapeutic aspects
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- Mosaicism of a novel variant in the ANKRD11 gene in a child with a mild KBG phenotype: A case report
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- Genome-wide associations, polygenic risk, and Mendelian randomization reveal limited interactions between John Henryism and cynicism
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- Phenotypic and cytogenetic features of an Iranian child with tetrasomy 18p syndrome: A case report
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- Epigenetics in the etiology and management of infertility
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- Celiac sprue - a cryptic disease: A case report
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- New era of cystic fibrosis: Full mutational analysis and personalized therapy
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- Chitosan DNA nanoparticles for oral gene delivery
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- Mutation in TNXB gene causes moderate to severe Ehlers-Danlos syndrome
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- Gene regulatory networks in atrial fibrillation
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- Oncofertility in adolescent and young adult hereditary cancer: Considerations for genetics professionals
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- Value of predictive bioinformatics in inherited metabolic diseases
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- Comparison of next generation sequencing-based and methylated DNA immunoprecipitation-based approaches for fetal aneuploidy non-invasive prenatal testing
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- Cell mediated gene therapy: A guide for doctors in the clinic
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- Genome variation in the trophoblast cell lifespan: Diploidy, polyteny, depolytenization, genome segregation
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- Preimplantation HLA typing: Practical tool for stem cell transplantation treatment of congenital disorders
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- Role of SOX2 in foregut development in relation to congenital abnormalities
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- Molecular genetics of gastric adenocarcinoma in clinical practice
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