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Harness Inherited Diseases
Through
Molecular Diagnosis & Genetic Counseling
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Our Mission
About Us
Our Diagnostic Services
Common Genetic & Infectious Diseases Diagnosis
Genetic & Inherited Diseases
β-Thalassemia
Sickle Cell Disease
Trisomy
Microcephaly
Epilepsy
Spinal Muscular Atrophy
Achondroplasia
Osteogenesis Imperfecta (OI)
Lipid Storage Disorder
Nephrotic Syndrome
Phocomelia Syndrome
Cystic Fibrosis
Tay Sachs
Retinitis Pigmentosa (RP)
Infectious Diseases
Hepatitis B (Qualitative & Quantitative)
Hepatitis C (Qualitative & Quantitative)
Hepatitis C (Genotyping)
NGS Based Disease Diagnosis
Tumors Syndromes
Cardiac Diseases
Blood and Immune disorders
Hearing Loss (Defness)
Epilepsy, Metabolic and Brain development disorders
Neurodegenerative Diseases
Neuromuscular Diseases
Kidney Diseases
Liver Diseases
Eye Diseases
Skin Diseases
Skeletal Disorders
Mitochondriopathies
Connective Tissue Diseases
Ion Channel Diseases
Ciliopathies
RASopathies
Rare Genetic Disorders Diagnosis
Adenosine Deaminase Deficiency (ADA)
Alpha-1 Antitrypsin Deficiency
Galactosemia
Huntington’s Disease (HD)
Maple Syrup Urine Disease (MSUD)
Neurofibromatosis Type-1 (NF1)
Pachyonychia Congenita (PC)
Phenylketonuria (PKU)
Severe Combined Immunodeficiency (SCID)
Smith-Lemli-Opitz Syndrome (SLOS)
Sanger / Direct Sequencing Services
Pre-Implantation IVF Embryo Genetic Screening
Genetic Counseling
Our Team
Research & Training
Molecular Biology
Bioinformatics
Biotechnology
Research Project Designing
Research Product / Technology Development
Primer / Probe Designing Services
Quantitative Life Sciences
Projects / Collaborations
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National
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2018-02-12T05:54:28+00:00
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