Ankita Sain

congenital fibre type disproportion central core myopathy nemaline myopathy central core disease congenital myopathy limb girdle muscular dystrophy occulopharyngeal muscular dystrophy dystrophy fascioscapulohumeral dystrophinopathies bmd becker's muscular dystrophy myotonic dystrophy dmd duchenne muscular dystrophy myotonia dystrophica muscular dystrophy emery driefuss muscular dystrophy inherited myopathies inherited myopathy single stranded conformational polymorphism (sscp) cold pr inverse pcr hot start pcr insutu pcr late pcr linear after the exponential pcr asymmetric pcr rt-pcr reverse transcriptase pcr dna polymerase primers dna template dna extension annealing taq polymerase denaturation pcr polymerase chain reaction blood component filters blood banking blood component leukocyte poor blood blood transfusion wbcs leukocyte reduced blood components leukocyte tissue microarray autostainer water bath automated drying automated embedding computer microtome laser microtome multisectioned retorts tissue processor microwave tissue processor microtomy microtome fluid exchange tissue processor tissue transfer tissue processor automated tissue processor tissue processor pathology histology automation in histopathology histopathology automation lymphoma classification of hodgkin's lymphoma hodgkin's rs cell reed sternberg cell hl hodgkin's disease hodgkin's lymphoma philadephia chromosome myeloproliferative neplasms chronic lymphocytic leukemia chronic myeloid leukemia cll cml chronic leukemia chronic ischemic heart disease pathology of myocardial infarction pathology of ischemic heart disease pathogenesis of mi pathogenesis of ihd pathogenesis of myocardial infarction pathogenesis if ischemic heart disease pathology of mi pathology of ihd stable angina unstable angina prinzmetal angina variants of angina angina pectoris angina mi heart attack myocardial infarction ihd ischemic heart disease ldh 5'nt ggt ast alt alp sgpt sgot lft liver function test men4 men 2b men 2a medullary carcinoma of thyroid sipple syndrome familial medullary thyroid carcinoma ret protooncogene ret gene pheochromocytoma medullary thyroid carcinoma multiple endocrine neoplasia 2 syndrome multiple endocrine neoplasia men 2 pathology of demyelinating diseases of cns demyelination cns myelin multiple sclerosis demyelinating diseases of cns demyelinating diseases enzymes in clinical pathology liver investigations liver pathology diagnostic liver pathology emzymology liver enzymes liver placenta genes genetics triple repeat abnormality