Category: Molecular Biology and Applied Genetics

Introduction DNA fingerprinting is a molecular technique used to identify individuals based on unique patterns in their DNA. Except for identical twins, every person has a unique DNA profile. The Read More ……..

Introduction Prenatal diagnosis refers to medical tests performed during pregnancy to detect genetic, chromosomal, and congenital abnormalities in the fetus. These diagnostic methods help identify inherited disorders and developmental defects Read More ……..

Introduction Mutation refers to a heritable and permanent change in the nucleotide sequence of genetic material (DNA or RNA). Mutations are fundamental biological events that generate genetic variation. Genetic variability Read More ……..

Introduction Haemophilia is a hereditary bleeding disorder caused by deficiency of specific coagulation factors. It results in prolonged or spontaneous bleeding due to defective blood clot formation. The disorder primarily Read More ……..

Introduction  Cystic fibrosis (CF) is a hereditary, autosomal recessive disorder. It primarily affects the respiratory, digestive, and sweat gland systems. The disease is caused by mutations in the CFTR (Cystic Read More ……..