New Clinical Genetics, first edition. Este artículo no está disponible.
5 valoraciones de Goodreads
Idioma: inglés
Editorial: Scion Publishing Ltd. (edition First Edition), 2006
- Primera edición
- Tapa blanda
- Usado

Librería: BooksRun, Philadelphia, PA, Estados Unidos de AmericaBooksRun
Vendedor de 5 estrellas
Vendedor de IberLibro desde 2 de febrero de 2016
No disponible
Tapa blanda
Condición: Usado - Bueno
EUR 7,16
Descripción del artículo del vendedor
It's a well-cared-for item that has seen limited use. The item may show minor signs of wear. All the text is legible, with all pages included. It may have slight markings and/or highlighting.
N° de ref. del artículo 1904842313-11-1
- Título
- New Clinical Genetics, first edition
- Autor
- Read, Andrew; Donnai, Dian
- Editorial
- Scion Publishing Ltd. (edition First Edition)
- Año de publicación
- 2006
- Estado
- Very Good
- Encuadernación
- Paperback
- Idioma
- inglés
- ISBN 10
- 1904842313
- ISBN 13
- 9781904842316
- Edición
- First Edition.
Aimed at medical students, genetic counsellors and clinical geneticists, this book provides the reader with a concise summary of post-genomic human genetics and guidance as to how our current understanding can be utilized in clinical practice. The book links genetics and clinical practice throughout using realistic case scenarios which are discussed throughout the book. Readers can take a problem-based approach to learning by working through each of the cases, or a more conventional approach by tackling each of the chapters in the order dictated by their course. The authors have based the book around the requirements of the NHS genetics education centre and the ASHG: which state that 'every physician who practices in the 21st century must have an in-depth knowledge of the principles of human genetics and their application to a wide variety of clinical problems'. The book benefits from a carefully designed format and layout to aid understanding. Each chapter includes self-assessment questions, separate boxes containing diagnostic methods and approaches, and common disease boxes. There are over 300 clinical photograph and figures, to further illustrate the points being discussed. Printed in full-colour throughout.
“Sinopsis” puede pertenecer a otra edición de este título.
Acerca del autor
Andrew Read (PhD, FRCPath, FMedSci) is Professor of Human Genetics at the University of Manchester. He is co-author of Strachan and Read's Human Molecular Genetics the leading advanced textbook on the subject. He established one of the first molecular genetic diagnostic services in the UK and has a long-standing interest in what genetic testing can and should, achieve. Dian Donnai (FRCP, FRCPCH, FMedSci) is Professor of Medical Genetics at the University of Manchester and Consultant Clinical Geneticist in the NW Regional Genetics Service. She is one of the world's leading authorities on clinical genetics, especially the study of dysmorphic syndromes, and is an advisor to many national and international bodies on the clinical application of genetics.
“Acerca de” puede pertenecer a otra edición de este título.