Non-Invasive Prenatal Screening of Rare Fetal Genetic Diseases
Language: English
Published by Elsevier Science, 2026
- Softcover
- New
Condition: New
£ 146.29
Quantity: 1 available
Add to basketItem description from seller
Provides a comprehensive overview of advancements in NIPS technology for detecting rare fetal genetic disordersDiscusses emerging trends, potential challenges, and ethical considerations in the application of NIPSHighlights practic.
Seller Inventory # 2769882905
- Title
- Non-Invasive Prenatal Screening of Rare Fetal Genetic Diseases
- Publisher
- Elsevier Science
- Publication year
- 2026
- Condition
- New
- Binding
- Soft cover
- Language
- English
- ISBN 10
- 0443276609
- ISBN 13
- 9780443276606
Researchers will find this to be a valuable resource for understanding and applying NIPS protocols in their work, while clinicians will benefit from practical insights on appropriate screening methods, interpreting NIPS results, and counseling expectant parents. This book is an essential resource for researchers in obstetrics and gynecology, genetic counselors, and professionals in the biotechnology and pharmaceutical industries. It equips readers with the knowledge and tools needed to advance their work and improve prenatal care practices.
- Provides a comprehensive overview of advancements in NIPS technology for detecting rare fetal genetic disorders
- Discusses emerging trends, potential challenges, and ethical considerations in the application of NIPS
- Highlights practical insights and research findings that enhance prenatal care and screening methods
- Explores the integration of advanced genomic methods in NIPS, including Next-Generation Sequencing and SNP analysis
- Offers case studies and clinical examples to illustrate the practical application of NIPS in prenatal screening
"Synopsis" may belong to another edition of this title.
About the Author
Professor Riyaz Ahmad Rather is an early-career researcher focused on non-invasive prenatal screening (NIPS). His work explores cell-free fetal DNA biomarkers for detecting various fetal anomalies. Some of his recent publications include studies on the role of cell-free fetal DNA in identifying RhD status using different exons, optimizing methods for isolating cell-free fetal DNA, and leveraging AI to detect cell-free fetal DNA contents.
Presently, his lab is engaged in research projects that utilize NIPS with cell-free fetal nucleic acids to detect chromosomal disorders.
"About the title" may belong to another edition of this title.
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