Für diesen Artikel ist leider kein Bild verfügbar.

Really Essential Medical Genetics

Buch | Softcover
144 Seiten
2007 | 6th Revised edition
Blackwell Publishing Ltd (Verlag)
978-1-4051-1330-4 (ISBN)
23,65 inkl. MwSt
  • Titel wird leider nicht erscheinen
  • Artikel merken
An illustrated introduction to medical genetics, this text deals with all the classical aspects of the subject. It is useful to both medical students and doctors who want to refresh their knowledge of the subject.
Fifth ed. reviews: "...a justifiably popular introductory text." The British Medical Journal. "...this book remains an indispensable introduction to a complex and rapidly changing field and will be useful to both medical students and doctors who want to refresh their knowledge of this increasingly important subject." Southampton Health Journal. "This book is an easy to read, well illustrated introduction to medical genetics. It deals nicely with all the classical aspects of the subject..." Black Bag, Medical Student's Society of Bristol University. "A huge improvement on the 4th edition, easier to read with more diagrams and photos...The layout is a lot better..." Mediscope, Manchester Medical Gazette.

Preface I General Principles of Medical Genetics I.1 Normal human inheritance I.2 Types of genetic disease I.3 Drawing the family tree I.4 Interpreting the family tree I.5 DNA analysis I.6 Chromosome analysis I.7 Sources of genetic information I.8 Referral for genetic assessment and counselling II Common Genetic Problems in Clinical Practice Presentation before or during pregnancy II.1 Infertility II.2 Recurrent miscarriages II.3 Increased risk of Down's syndrome after screening II.4 Increased risk of neural tube defect after screening II.5 Increased risk of cystic fibrosis after screening II.6 Family history of Down's syndrome II.7 Family history of neural tube defect II.8 Familiy history of cystic fibrosis II.9 Family history of muscular dystrophy II.10 Family history of major learning difficulties II.11 Family history of multiple congenital malformations Presentation in childhood II.12 Diagnosis following neonatal screening (PKU, CF, hypothyroidism, cong deafness) II.13 Congenital malformations II.14 Short stature II.15 Muscle weakness II.16 Learning difficulties (?epilepsy, neoplasia) Presentation in adulthood II17 Cancer II.18 Vascular disease II.19 Dementia II.20 Arthritis II.21 Muscle weakness (? ) III Clincal case scenarios CCS1 Family tree construction CCS2 Interpreting the family tree (several) CCS3 Unexpected findings at amniocentesis (Turners Klinefelters appt balalnced) CCS 4 Sources of genetic information (Meckels) CCS5 recurrent miscarriages in opposite side CCS More than one disease CCS Family history of Down's syndrome CCS Family history of neural tube defect in a mother CCS Familiy history of cystic fibrosis (unknown mutation) CCS Family history of muscular dystrophy (x2) CCS Family history of major learning difficultiesCCS Family history of multiple congenital malformations (examples) CCS Family history of ovarian cancer florid without mutation, grey CCS Huntington's disease and age-dependent penetrance CCS Ethics+++ CCS Haemoglobinopathy/ethnic origin CCS Maternal PKU CCS Us diagnosed abn CCS Paternity issues Klinefelter/CF

Zusatzinfo 100
Verlagsort Oxford
Sprache englisch
Maße 219 x 276 mm
Themenwelt Studium 2. Studienabschnitt (Klinik) Humangenetik
ISBN-10 1-4051-1330-8 / 1405113308
ISBN-13 978-1-4051-1330-4 / 9781405113304
Zustand Neuware
Haben Sie eine Frage zum Produkt?
Mehr entdecken
aus dem Bereich
Eine sehr persönliche Geschichte | Der New York Times-Bestseller

von Siddhartha Mukherjee

Buch | Softcover (2023)
Ullstein Taschenbuch Verlag
21,99
Die revolutionäre Medizin von morgen (Lifespan)

von David A. Sinclair; Matthew D. LaPlante

Buch | Softcover (2020)
DuMont Buchverlag
16,00