Molecular detection of inherited haematological disorder of human

摘要

A human disease studies on molecular level and its diagnostics are result of our approach towards our aim to look after patients in their absolute genetic needs from counselling to DNA profiling for disease prevention, bytaking entire genetic tests from hereditarydiseases to infectious diseases from introduction of individualized medicines to prenatal diagnosis from noninvasive methods. Molecular Diagnosis of disease is very useful way to detect abnormalities in DNAlevel. The technique is rapid, cost effective, accurate and gold standard.Various diseases i.e. Infectious (Viral, Bacterial, Fungal), Inherited and malignancies can be detected in early stage and medication can be started that save time, money and life.