BSE636A - Human Molecular Genetics

Simple Mendelian traits; Loss of function mutations; Gain of function mutations; Gene interactions; Dynamic mutations; Genetics of neoplasia; Genomic imprinting and human disease; X inactivation and DNA methylation; Gene mapping and positional cloning; Muti factorial inheritance; Genetics of behavioral disorders; Pharmaco genetics and biochemical genetics; Animal models in human genetics: Methods used for diagnosis and detection of gene mutations; Gene Therapy.