Oxford Desk Reference: Clinical Genetics
Seiten
2005
Oxford University Press (Verlag)
978-0-19-262896-1 (ISBN)
Oxford University Press (Verlag)
978-0-19-262896-1 (ISBN)
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This important new book provides a practical, easy-to-use guide to clinical consultation in genetics, covering the process of diagnosis, investigation, management, and counselling for patients. All genetic conditions are covered as well as referral categories for a clinical genetic opinion.
The first in a brand new series of easy-to-use guides, this book is set to become the bible for clinical consultation in genetics. It covers the process of diagnosis, investigation, management, and counselling for patients. Most of the topics fit onto a double-page spread ensuring that the book is an accessible, quick reference for the clinic or hospital consultation. Where available, diagnostic criteria for specific conditions are included as well as contact details for support groups. The book is well illustrated and has an up-to-date bibliography and glossaries of terms used in genetics and dysmorphology. The authors have used their experience to devise a practical clinical approach to many common genetic referrals, both out patient and ward based. The most common Mendelian disorders, chromosomal disorders, congenital anomalies and syndromes are all covered. In addition there are chapters on familial cancer and pregnancy-related topics such as foetal anomalies, teratogens, prenatal and pre-implantation diagnosis. The book also provides information on the less common situations, where management is particularly complex, or important genetic concepts are illustrated.
The first in a brand new series of easy-to-use guides, this book is set to become the bible for clinical consultation in genetics. It covers the process of diagnosis, investigation, management, and counselling for patients. Most of the topics fit onto a double-page spread ensuring that the book is an accessible, quick reference for the clinic or hospital consultation. Where available, diagnostic criteria for specific conditions are included as well as contact details for support groups. The book is well illustrated and has an up-to-date bibliography and glossaries of terms used in genetics and dysmorphology. The authors have used their experience to devise a practical clinical approach to many common genetic referrals, both out patient and ward based. The most common Mendelian disorders, chromosomal disorders, congenital anomalies and syndromes are all covered. In addition there are chapters on familial cancer and pregnancy-related topics such as foetal anomalies, teratogens, prenatal and pre-implantation diagnosis. The book also provides information on the less common situations, where management is particularly complex, or important genetic concepts are illustrated.
PART 1: INTRODUCTION; PART 2: CLINICAL APPROACH; PART 3: COMMON CONSULTATIONS; PART 4: CANCER; PART 5: CHROMOSOMES; PART 6: PREGNANCY AND FERTILITY; APPENDIX
| Erscheint lt. Verlag | 1.7.2005 |
|---|---|
| Reihe/Serie | Oxford Desk Reference |
| Zusatzinfo | numerous line figures |
| Verlagsort | Oxford |
| Sprache | englisch |
| Gewicht | 1594 g |
| Themenwelt | Medizin / Pharmazie ► Medizinische Fachgebiete ► Gynäkologie / Geburtshilfe |
| Medizin / Pharmazie ► Medizinische Fachgebiete ► Onkologie | |
| Medizin / Pharmazie ► Medizinische Fachgebiete ► Pädiatrie | |
| Studium ► 2. Studienabschnitt (Klinik) ► Humangenetik | |
| ISBN-10 | 0-19-262896-8 / 0192628968 |
| ISBN-13 | 978-0-19-262896-1 / 9780192628961 |
| Zustand | Neuware |
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