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9780815345893

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Human Molecular Genetics
av Tom Strachan and Andrew P Read
Häftad bok. Boca Raton, Florida: CRC Press, Taylor and Francis Group. 5 uppl. 2020. xiii, (1), 770 sidor.

Mer om ISBN 9780815345893

Nyskick. Fifth edition. Ny/oläst. Vikt 2,3 kg.

Säljare: Sundblom, Erik (företag)

Inrikes enhetsfrakt Sverige: 62 SEK

ISBN

9780815345893

Titel

Human molecular genetics

Författare

Strachan, Tom

Utgivningsår

2019

Bandtyp

Paperback

Språk

English

Baksidestext

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.

Boca Raton, Florida: CRC Press, Taylor and Francis Group 5 9780815345893

ISBN: 9780815345893
Titel: Human molecular genetics
Författare: Strachan, Tom
Utgivningsår: 2019
Bandtyp: Paperback
Språk: English

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.