Human Molecular Genetics

Human Molecular Genetics

Human Molecular Genetics has been carefully crafted over successive editions to provide an authoritative introduction to the molecular aspects of human genetics, genomics and cell biology.Maintaining the features that have made previous editions so popular, this fifth edition has been completely updated in line with the latest developments in the field. Older technologies such as cloning and hybridization have been merged and summarized, coverage of newer DNA sequencing technologies has been expanded, and powerful new gene editing and single-cell genomics technologies have been added. The coverage of GWAS, functional genomics, stem cells, and disease modeling has been expanded. Greater focus is given to inheritance and variation in the context of populations and on the role of epigenetics in gene regulation. Key features:Fully integrated approach to the molecular aspects of human genetics, genomics, and cell biologyAccessible text is supported and enhanced throughout by superb artwork illustrating the key concepts and mechanismsSummary boxes at the end of each chapter provide clear learning pointsAnnotated further reading helps readers navigate the wealth of additional information in this complex subject and provides direction for further studyReorganized into five sections for improved access to related topicsAlso new to this edition ? brand new chapter on evolution and anthropology from the authors of the highly acclaimed Human Evolutionary GeneticsA proven and popular textbook for upper-level undergraduates and graduate students, the new edition of Human Molecular Genetics remains the ?go-to? book for those studying human molecular genetics or genomics courses around the world.

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Editorial Reviews

Review

The authors have improved their contribution to the field of human genetics teaching with every edition. The book’s design makes it unique and it provides a wonderful platform for student learning. It is a complex subject.

Luis F Escobar is a doctor at the Peyton Manning Children’s Hospital.

–This text refers to an out of print or unavailable edition of this title.

About the Author

The man is Tom Strachan. He is a Fellow of the Academy of Medical Sciences and a member of the Royal Society of Edinburgh. From 2001 to 2009, he was the Scientific Director of the Institute of Human Genetics. Tom?s early research interests were in multigene family evolution and interlocus sequence exchange. He became interested in medical genetics while pursuing the latter. His research focuses on developmental disorders and control genes.

Andrew Read. He is a Fellow of the Academy of Medical Sciences. Andrew was concerned about making the benefits of DNA technology available to people with genetic problems. He was the founder chairman of the British Society for Human Genetics, the main professional body in this area, and established one of the first DNA diagnostic laboratories in the UK over 20 years ago. His research focuses on the pathology of hereditary hearing loss.

The European Society of Human Genetics Education Award was given to Drs. Strachan and Read.

–This text refers to an out of print or unavailable edition of this title.

Additional information

Best Sellers Rank

#676,719 in Kindle Store (See Top 100 in Kindle Store) #73 in Cell Biology (Kindle Store) #80 in Molecular Biology (Kindle Store) #198 in Genetic Science

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