Updated to reflect the newest changes in genetics, Thompson & Thompson's Genetics in Medicine returns as one of the most favored texts in this fascinating and rapidly evolving field. By integrating the classic principles of human genetics with mo ...view more
Updated to reflect the newest changes in genetics, Thompson & Thompson's Genetics in Medicine returns as one of the most favored texts in this fascinating and rapidly evolving field. By integrating the classic principles of human genetics with modern molecular genetics, this medical reference book utilizes a variety of learning tools to help you understand a wide range of genetic disorders. This Student Consult eBook version allows you to search all of the text, figures, and references from the book on a variety of devices. You'll also access USMLE-style and multiple choice questions.
Updated to reflect the newest changes in genetics, Thompson & Thompson's Genetics in Medicine returns as one of the most favored texts in this fascinating and rapidly evolving field. By integrating the classic principles of human genetics with modern molecular genetics, this medical reference book utilizes a variety of learning tools to help you understand a wide range of genetic disorders. This Student Consult eBook version allows you to search all of the text, figures, and references from the book on a variety of devices. You'll also access USMLE-style and multiple choice questions.
New to this edition
Immerse yourself in updated graphics
, full-color text, illustrations, line diagrams, and clinical photos of genetic diseases.
Explore the latest genetic content available in order to remain up to date on the most current trends in the field.
Take advantage of a double-page clinical case study section that demonstrates and reinforces general principles of disease inheritance, pathogenesis, diagnosis, management, and counseling.
Enhance your critical thinking skills and better retain information. Each chapter ends with up to 5 quick genetic "problems" related to what has just been reviewed, with answers provided in the back of the book.
Student Consult eBook version included with purchase. This enhanced eBook experience allows you to search all of the text, figures, and references from the book on a variety of devices. You'll also access USMLE-style and multiple choice questions.
Key Features
Acquire the state-of-the-art knowledge you need on the latest advances in molecular diagnostics, the Human Genome Project, pharmacogenetics, and bio-informatics.
Better understand the relationship between basic genetics and clinical medicine with a variety of clinical case studies.
Recognize a wide range of genetic disorders with visual guidance from more than 240 dynamic illustrations and high-quality photos.
Author Information
By Robert L. Nussbaum, MD, FACP, FACMG, Holly Smith Chair of Medicine and Science, Professor of Medicine, Neurology, Pediatrics and Pathology, Department of Medicine and Institute for Human Genetics, University of California San Francisco, San Francisco, California; Roderick R. McInnes, CM, MD, PhD, FRS(C), FCAHS, FCCMG, Alva Chair in Human Genetics, Canada Research Chair in Neurogenetics, Professor of Human Genetics and Biochemistry, Director, Lady Davis Institute, Jewish General Hospital, McGill University, Montreal, Quebec, Canada and Huntington F Willard, Chief Scientific Officer, Genome Medical, Inc., South San Francisco, CA, USA
Bring it with you - The Bookshelf app allows you to access books on your laptop, tablet or mobile, so your ebooks go where ever you are - online or offline.
Take notes - Highlight, bookmark and take notes and highlights automatically stay in sync no matter where you make them.
Listen to eBooks - When you need to go screenless, the Text-to-speech tool will read your book aloud.
Powerful search - The searching capabilities allow you to search keywords through all your eBooks, the entire Bookshelf Library and well as on Wikipedia.
Ecological - Manage your environmental impact with paperless books.
How to read your VitalSource eBooks
Purchase your VitalSource eBook on the Elsevier Health site
https://www.uk.elsevierhealth.com/thompson-thompson-genetics-in-medicine-9780323392051.html70210Thompson & Thompson Genetics in Medicinehttps://www.uk.elsevierhealth.com/media/catalog/product/9/7/9780323392051_8.jpg28.4937.99GBPInStock/Medicine and Surgery/Genetics /eBooks/Medical Students/Medical education10475525504024672471745310000514512010516<p>Updated to reflect the newest changes in genetics, <b><i>Thompson & Thompson's Genetics in Medicine</b></i> returns as one of the most favored texts in this fascinating and rapidly evolving field. By integrating the <b>classic principles of human genetics</b> with <b>modern molecular genetics</b>, this medical reference book utilizes a variety of learning tools to help you understand a wide range of genetic disorders. This Student Consult eBook version allows you to search all of the text, figures, and references from the book on a variety of devices. You'll also access <b>USMLE-style</b> and <b>multiple choice questions</b>.</p> <p>Updated to reflect the newest changes in genetics, <b><i>Thompson & Thompson's Genetics in Medicine</b></i> returns as one of the most favored texts in this fascinating and rapidly evolving field. By integrating the <b>classic principles of human genetics</b> with <b>modern molecular genetics</b>, this medical reference book utilizes a variety of learning tools to help you understand a wide range of genetic disorders. This Student Consult eBook version allows you to search all of the text, figures, and references from the book on a variety of devices. You'll also access <b>USMLE-style</b> and <b>multiple choice questions</b>.</p>00add-to-cart97803233920512015ProfessionalBy Robert L. Nussbaum, MD, FACP, FACMG, Roderick R. McInnes, CM, MD, PhD, FRS(C), FCAHS, FCCMG and Huntington F Willard20168E-BookOtherApprox. 543 illustrations (543 in full color)Elsevier5285 Jun 2015IN STOCKBy <STRONG>Robert L. Nussbaum</STRONG>, MD, FACP, FACMG, Holly Smith Chair of Medicine and Science, Professor of Medicine, Neurology, Pediatrics and Pathology, Department of Medicine and Institute for Human Genetics, University of California San Francisco, San Francisco, California; <STRONG>Roderick R. McInnes</STRONG>, CM, MD, PhD, FRS(C), FCAHS, FCCMG, Alva Chair in Human Genetics, Canada Research Chair in Neurogenetics, Professor of Human Genetics and Biochemistry, Director, Lady Davis Institute, Jewish General Hospital, McGill University, Montreal, Quebec, Canada and <STRONG>Huntington F Willard</STRONG>, Chief Scientific Officer, Genome Medical, Inc., South San Francisco, CA, USAeBooksNoNoNoNoPlease SelectPlease SelectPlease Select
