Biochemistry by jamesadmin | Aug 21, 2019 | Uncategorized Current Status Not Enrolled Price Closed Get Started This quiz sections is currently closed My Quiz HistoryDashboard Quiz Sections Content Biochemistry- Genetics- Section XI.2- Klinefelter’s Syndrome Biochemistry-Metabolism-Section XX.11 – Vitamin D Biochemistry- Genetics- Section XII- Microdeletion Syndromes Biochemistry-Lab techniques-Section I-PCR Biochemistry-Metabolism-Section XX.12 – Vitamin E Biochemistry- Genetics- Section XII.1- Cri-du-chat Syndrome Biochemistry-Metabolism-Section XX.14 – Zinc Biochemistry- Genetics- Section XII.2- Williams Syndrome Biochemistry- Genetics- Section XII.3- Digeorge Syndrome Biochemistry-Lab techniques-Section II-Blotting Procedures Biochemistry-Molecular-Section I-DNA Replication Biochemistry-Molecular-Section II-DNA Repair Biochemistry-Cellular-Section I-Cell Cycle Biochemistry-Cellular-Section II-Cell Structure Biochemistry-Molecular-Section III-Transcription Biochemistry-Cellular-Section III-Connective Tissue Biochemistry-Lab techniques-Section III-Flow Cytometry Biochemistry-Molecular-Section IV-Translation Biochemistry- Metabolism-Section I- Hexokinase and Glucokinase metabolism Biochemistry-Genetics-Section VII.2-Rett Syndrome Biochemistry-Molecular-Section V-DNA Mutations Biochemistry-Lab techniques-Section IV-Microarrays and ELISA Biochemistry-Metabolism-Section XX.8 – Cobalamin (B12) Biochemistry-Genetics-Section VIII-Autosomal Recessive Diseases Biochemistry-Metabolism-Section XX.9 – Vitamin C Biochemistry-Lab techniques-Section V-Karyograms and FISH Biochemistry-Metabolism-Section XX.13 – Vitamin K Biochemistry-Genetics-Section IX-Trinucleotide repeat disorders Biochemistry-Genetics- Section IX.1-Huntington Disease Biochemistry-Lab techniques-Section VI-CRISPR/Cas9 & Molecular Cloning Biochemistry-Genetics-Section IX.2-Myotonic Dystrophy Biochemistry-Metabolism-Section III – Pyruvate Biochemistry-Genetics-Section IX.3-Fragile X Syndrome Biochemistry-Metabolism-Section VII.1 – Von Gierke & Cori Disease Biochemistry – Metabolism- Section II – Glycolysis Biochemistry-Genetics-Section IX.4-Friedrich Ataxia Biochemistry-Metabolism-Section VII.2 – Pompe & Mcardle Disease Biochemistry-Metabolism-Section VIII – Fructose Metabolism Biochemistry-Genetics-Section X-Autosomal Trisomies Biochemistry-Metabolism-Section X – HMP Shunt Biochemistry-Genetics-Section X.1-Down Syndrome Biochemistry-Metabolism-Section XI – Fat Metabolism Biochemistry-Genetics-Section I- Genetics Overview Biochemistry-Metabolism-Section XX.4 – Pantothenic Acid (B5) Biochemistry-Genetics-Section II-Imprinting and Uniparental Disomy Biochemistry-Metabolism-Section V – ETC Biochemistry-Metabolism-Section XIX.4 – Krabbe Disease Biochemistry-Metabolism-Section XIX.3 – Metachromatic Leukodystrophy Biochemistry-Metabolism-Section XIX.2 – Fabry Disease Biochemistry-Metabolism-Section XIX.1 – Tay-Sachs & Niemann-Pick Disease Biochemistry-Metabolism-Section XIX – Lysosomal Storage Diseases Biochemistry-Metabolism-Section IV – TCA Cycle Biochemistry-Metabolism-Section XIX.6 – Hurler & Hunter Syndrome Biochemistry-Metabolism-Section XIX.5 – Gaucher Disease Biochemistry-Genetics-Section III- Linkage Disequilibrium Biochemistry-Metabolism-Section XII – Ketones Biochemistry-Metabolism-Section IX – Galactose Biochemistry-Metabolism-Section VI – Gluconeogenesis Biochemistry-Genetics-Section IV-Pedigrees Biochemistry-Metabolism-Section XIII – Ethanol Biochemistry-Genetics-Section VI.1-Autosomal Dominant Disease Biochemistry-Metabolism-Section VII – Glycogen Biochemistry-Genetics-Section VII.1-X-Linked Recessive Diseases Biochemistry- Genetics- Section X.2- Edwards Syndrome Biochemistry-Metabolism-Section XIV – Lipid Transport Biochemistry-Metabolism-Section XV – Homocysteine Biochemistry-Genetics-Section V-Hardy-Weinberg Principle Biochemistry-Metabolism-Section XX.3 – Niacin (B3) Biochemistry-Metabolism-Section XVI – Purines & Pyrimidines Biochemistry- Genetics- Section X.3- Patau Syndrome Biochemistry-Metabolism-Section XX.5 – Pyridoxine (B6) Biochemistry- Genetics- section XI- Sex Chromosome Disorders Biochemistry-Genetics-Section VI-Autosomal Dominant Disease Biochemistry-Metabolism-Section XX.1 – Thiamine (B1) Biochemistry-Metabolism-Section XX.6 – Biotin (B7) Biochemistry-Metabolism-Section XVII – Ammonia Biochemistry- Genetics- Section XI. 1- Turner Syndrome Biochemistry-Metabolism-Section XX.7 – Folate (B9) Biochemistry-Metabolism-Section XVIII – Amino Acids Biochemistry-Genetics-Section VII-X-Linked Recessive Diseases Biochemistry-Metabolism-Section XX.2 – Riboflavin (B2) Biochemistry-Metabolism-Section XX – Nutrition Biochemistry-Metabolism-Section XX.10 – Vitamin A
