Genetic Biochemical Disorders
Seiten
1985
Oxford University Press (Verlag)
978-0-19-261193-2 (ISBN)
Oxford University Press (Verlag)
978-0-19-261193-2 (ISBN)
- Titel ist leider vergriffen;
keine Neuauflage - Artikel merken
Rapid progress has been made in recent years in both the diagnostic methodology for and the therapy of genetic biochemical disorders. This book serves as a comprehensive source of information for clinicians and laboratory staff.
The very rapid advances in biochemical technology recently have helped identify the basic defect in about 250 genetic disorders. Early precise diagnosis is essential before therapy can be identified which will lead to survival and normal development. This book describes clinical, pathological, and biochemical features, diagnostic methodology, and the necessary data for genetic counselling.
The very rapid advances in biochemical technology recently have helped identify the basic defect in about 250 genetic disorders. Early precise diagnosis is essential before therapy can be identified which will lead to survival and normal development. This book describes clinical, pathological, and biochemical features, diagnostic methodology, and the necessary data for genetic counselling.
| Erscheint lt. Verlag | 12.12.1985 |
|---|---|
| Reihe/Serie | Oxford Monographs on Medical Genetics |
| Zusatzinfo | 78figs.11tabs. |
| Verlagsort | Oxford |
| Sprache | englisch |
| Maße | 150 x 230 mm |
| Gewicht | 1330 g |
| Themenwelt | Studium ► 2. Studienabschnitt (Klinik) ► Humangenetik |
| ISBN-10 | 0-19-261193-3 / 0192611933 |
| ISBN-13 | 978-0-19-261193-2 / 9780192611932 |
| Zustand | Neuware |
| Haben Sie eine Frage zum Produkt? |
Mehr entdecken
aus dem Bereich
aus dem Bereich
Eine sehr persönliche Geschichte | Der New York Times-Bestseller
Buch | Softcover (2023)
Ullstein Taschenbuch Verlag
CHF 30,75
Die revolutionäre Medizin von morgen (Lifespan)
Buch | Softcover (2020)
DuMont Buchverlag
CHF 22,40
Buch | Softcover (2022)
John Wiley & Sons Inc (Verlag)
CHF 169,95
