Welcome to Personal Website of Dr Manjeet Kaur, Genetics Specialist from India

<p>Welcome to Personal Website of Dr Manjeet Kaur, Genetics Specialist from India</p><p>Dr. Manjeet Kaur, Genetics Specialist, Research work: Immunology, Genetics, Molecular Biology, Enzymology, Newborn Screening. Malaria Immunology.Studies on Giardia Lamblia.Epidemiology of E.histolytica by zymodeme study and serology. Study on Medico-Genetic problems in tribal communities. Biochemical Genetic Disorders in India. Disorders of Amino-acid Metabolism, Organic acids, Fatty acid disorders, - Disorders of Galactose Metabolism - Mucoploysaccharidoses (MPS) Disease, - Enzyme assays for Lysosomal Enzyme Disorders, - Prenatal Diagnosis, - Estimation of Ceruloplasmin and Alpha1-antitrypsin : for metabolic liver disorders. Triple Marker Test for Prenatal diagnosis of Down's syndrome and NTD</p><p>Portosystemic shunt , Citrin deficiency , Galactokinase , Neurological , learning problems , Renal Fanconi syndrome , Seizures , Diarrhoea , Vomitting , Liver dysfunction, Liver foundation, Irritabilty, Lethargy, GALT, Uridyltransferase , Galactosemia , Oatbran , Legumes , Soybeans , Biotin, Alopecia , Skin rash , Optic atrophy , Hearing loss , Seizures , Hypotonia , Ataxia , Biotinidase deficiency, IRT, Molecular Genetic Testing, DNA Analysis , Sweat Test, CF babies, Newborn Screening, cervix , Male sterility, Male infertility, Irregular menstruation , Delayed sexual development , Liver disease, Pancreatitis , Diabetes , Gall stones , Stomach pain , Poor growth , Heart enlargement , Nasal polyps , pneumothorax, hemoptysis, pneumonia , wheezing , Chronic cough , Congenital, Cystic Fibrosis , Adrenal Hyperplasia, X-Linked , Autosomal Recessive , Autosomal Dominant, Single Gene Disorders, genetic disorders , Genetic Councellors, gene , DNA , Trait, Heredity, Protein, Chromosome, Genetics , Delhi, Dr Lal PathLabs Pvt Ltd, India, www.DrManjeet.com , Dr Manjeet Kaur, </p>