Part genetics primer and part memoir, this is a richly compelling read. - BooklistMy niece was 36, newly married, and ;on top of the world, when she collapsed and died. Her autopsy report caused us to panicthere was something in our blood that cou...Loe edasi...
Part genetics primer and part memoir, this is a richly compelling read. - BooklistMy niece was 36, newly married, and ;on top of the world, when she collapsed and died. Her autopsy report caused us to panicthere was something in our blood that cou...Loe edasi...
(Ilmumisaeg: 15-Nov-2024, EPUB+DRM, Kirjastus: Taylor & Francis Ltd, ISBN-13: 9781040282274)
Recent years have seen rapid advances in our understanding of genetic diseases in terms of their molecular origins. The book focuses on DNA mutations which give rise to abnormalities of protein structure and function in genetic disease....Loe edasi...
(Ilmumisaeg: 15-Nov-2024, PDF+DRM, Kirjastus: Taylor & Francis Ltd, ISBN-13: 9781040285985)
Recent years have seen rapid advances in our understanding of genetic diseases in terms of their molecular origins. The book focuses on DNA mutations which give rise to abnormalities of protein structure and function in genetic disease....Loe edasi...
After years of hearing that she was an inspiration to family and friends, Heather decided to strive to inspire a larger audience by writing. Citing a lifetime of personal experiences, she gives her readers an inside look at her world of insane medica...Loe edasi...
Epigenetics in Human Disease, Third Edition examines the diseases and conditions on which we have advanced knowledge of epigenetic mechanisms, such as cancer, autoimmune disorders, aging, metabolic disorders, neurobiological disorders and cardiovascu...Loe edasi...
Epigenetics in Human Disease, Third Edition examines the diseases and conditions on which we have advanced knowledge of epigenetic mechanisms, such as cancer, autoimmune disorders, aging, metabolic disorders, neurobiological disorders and cardiovascu...Loe edasi...
Genetic Steroid Disorders, Second Edition targets adult and pediatric endocrinologists, clinical geneticists, genetic counselors, reproductive endocrinologists, neonatologists, urologists, and psychoendocrinologists. It is designed to assist these sp...Loe edasi...
Genetic Steroid Disorders, Second Edition targets adult and pediatric endocrinologists, clinical geneticists, genetic counselors, reproductive endocrinologists, neonatologists, urologists, and psychoendocrinologists. It is designed to assist these sp...Loe edasi...
This book explores the basic concepts of genetics and heredity in human diseases. It discusses techniques like RT-PCR, karyotyping, DNA/RNA extraction, RFLP, DNA sequencing and electrophoresis, which will be helpful in clinical diagnostics for patien...Loe edasi...
This book describes the historical context of colorectal cancer predisposition syndromes and the latest knowledge relating to each of the known hereditary colorectal cancer predisposition syndromes. There is a particular focus on the management of ea...Loe edasi...
Kim Zeidler hat Psoriasis, seitdem sie 4 Jahre alt ist. Das erste Mal kurze Hosen trug sie allerdings erst mit 30, weil sie sich für die weißen Flecken auf ihrer Haut, die die Schuppenflechte verursacht, so geschämt hat. Dank des positiven Zuspruc...Loe edasi...
Kim Zeidler hat Psoriasis, seitdem sie 4 Jahre alt ist. Das erste Mal kurze Hosen trug sie allerdings erst mit 30, weil sie sich für die weißen Flecken auf ihrer Haut, die die Schuppenflechte verursacht, so geschämt hat. Dank des positiven Zuspruc...Loe edasi...
Kathy Steligo, Sue Friedman, Allison W. Kurian, Matthew Boland Yurgelun
(Ilmumisaeg: 27-Sep-2022, PDF+DRM, Kirjastus: Johns Hopkins University Press, ISBN-13: 9781421444277)
The most comprehensive guide available on hereditary cancers, from understanding risk, prevention, and genetic counseling and testing to treatment, quality of life, and more.Up to 10 percent of cancers are caused by inherited mutations in specific ge...Loe edasi...
Kathy Steligo, Sue Friedman, Allison W. Kurian, Matthew Boland Yurgelun
(Ilmumisaeg: 27-Sep-2022, EPUB+DRM, Kirjastus: Johns Hopkins University Press, ISBN-13: 9781421444277)
The most comprehensive guide available on hereditary cancers, from understanding risk, prevention, and genetic counseling and testing to treatment, quality of life, and more.Up to 10 percent of cancers are caused by inherited mutations in specific ge...Loe edasi...
(Ilmumisaeg: 12-May-2022, PDF+DRM, Kirjastus: Oxford University Press, ISBN-13: 9780192593290)
Containing concise, updated, and easy-to-use summaries on a comprehensive range of clinical scenarios and conditions encountered by paediatricians and multi-disciplinary professionals in their everyday practice, this new edition of Neurodisability an...Loe edasi...
(Ilmumisaeg: 12-May-2022, EPUB+DRM, Kirjastus: Oxford University Press, ISBN-13: 9780192593306)
Containing concise, updated, and easy-to-use summaries on a comprehensive range of clinical scenarios and conditions encountered by paediatricians and multi-disciplinary professionals in their everyday practice, this new edition of Neurodisability an...Loe edasi...
(Ilmumisaeg: 01-Jul-2021, MP3, Kirjastus: Random House, ISBN-13: 9781473597167)
Brought to you by Penguin.Welcome to a revolution in the science of human health. Imagine...- Knowing years in advance whether you are likely to get certain cancers- Having a bespoke understanding of your individual genes, organs and cells- Following...Loe edasi...
A big-picture forecast of how medicine stands on the threshold of a revolution that will radically change all of our lives The TimesWelcome to a revolution in the science of you. This landmark new book from award-winning scientist Daniel M. Davis e...Loe edasi...
(Ilmumisaeg: 05-Jan-2021, PDF+DRM, Kirjastus: Springer-Verlag Berlin and Heidelberg GmbH & Co. KG, ISBN-13: 9783662624500)
Dieses Buch analysiert die Rechtslage im Hinblick auf die heterologe Insemination in Deutschland, Österreich und der Schweiz. Den Schwerpunkt bildet dabei die Untersuchung des im Jahre 2018 in Deutschland in Kraft getretenen Samenspenderregiste...Loe edasi...
