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The Journal of Clinical Genetics and Genomics places special focus on the underlying cause of inherited diseases and genetic syndromes such as: Fragile-X Syndrome, Thalassemia, Huntington’s disease, Cystic fibrosis, Down syndrome, Mitochiondrial Disease, Muscular Dystrophy, and Patau Syndrome. Special impetus is placed on studies dealing with molecular approaches in understanding the disease pathogenesis.
Studies involving genomic studies such as: genetic mapping by next generation sequencing techniques, RNA-Sequencing, ChIP-Sequencing, and microarray are highly solicited. Further, studies concerned with diagnostic techniques such as RAPD and RFLPfor screening mutations or identifying polymorphisms are also solicited. The scope of the Journal of Clinical Genetics and Genomics also encompasses articles from the fields of neurogenetics, cancer genetics, medical genetics, biochemical genetics, population genetics, genetic epidemiology, and immunogenetics.