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 ● Páginas 175 ● ISBN 9781527588790 ● Editora Cambridge Scholars Publishing ● Publicado 2022 ● Carregável 3 vezes ● Moeda EUR ● ID 9279824 ● Proteção contra cópia Adobe DRM
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