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Cover for 9780896037168 Cover for 9780896037212 Cover for 9781489942128 Cover for 9781617371509
DNA Sequencing Protocols
cover image for 9781489942128
Product Description: Colin Graham and a team of leading investigators and expert clinical scientists update the acclaimed first edition with a collection of powerful, up-to-date PCR-based methods for DNA sequencing, many suitable for human genome sequencing and mutation detection in human disease...read more
By Colin A. Graham (editor) and Alison J. M. Hill (editor)
See complete details on each edition (4 editions listed)

Hardcover:

9780896037168 | 2 sub edition (Humana Pr Inc, January 1, 2001), cover price $104.50 | About this edition: Colin Graham and a team of leading investigators and expert clinical scientists update the acclaimed first edition with a collection of powerful, up-to-date PCR-based methods for DNA sequencing, many suitable for human genome sequencing and mutation detection in human disease.

Paperback:

9781489942128 | 2 edition (Humana Pr Inc, September 1, 2013), cover price $99.00 | About this edition: Colin Graham and a team of leading investigators and expert clinical scientists update the acclaimed first edition with a collection of powerful, up-to-date PCR-based methods for DNA sequencing, many suitable for human genome sequencing and mutation detection in human disease.
9781617371509 | 2 edition (Humana Pr Inc, December 12, 2011), cover price $149.00 | About this edition: Colin Graham and a team of leading investigators and expert clinical scientists update the acclaimed first edition with a collection of powerful, up-to-date PCR-based methods for DNA sequencing, many suitable for human genome sequencing and mutation detection in human disease.
9780896037212 | 2 spi edition (Humana Pr Inc, January 1, 2001), cover price $149.00 | About this edition: Colin Graham and a team of leading investigators and expert clinical scientists update the acclaimed first edition with a collection of powerful, up-to-date PCR-based methods for DNA sequencing, many suitable for human genome sequencing and mutation detection in human disease.

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