This book explores the basic concepts of genetics and heredity in human diseases. It discusses techniques like RT-PCR, karyotyping, DNA/RNA extraction, RFLP, DNA sequencing and electrophoresis, which will be helpful in clinical diagnostics for patients. The book also considers developmental anomalies and birth defects, as well as the potential for folate metabolism to act as a "risk factor" in genetic disorders.
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Formato PDF ● Pagine 175 ● ISBN 9781527588790 ● Casa editrice Cambridge Scholars Publishing ● Pubblicato 2022 ● Scaricabile 3 volte ● Moneta EUR ● ID 9279824 ● Protezione dalla copia Adobe DRM
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