The year in human and medical genetics
Jean-Laurent Casanova, Mary Ellen Conley, Luigi Notarangelo · 2011
על הספר
The genetic dissection of human primary immunodeficiency is expanding at full speed, in at least two directions. Some investigators pursue the dissection of well-known clinical phenotypes, for which the count of genetic etiologies seems to be endless, whereas others begin the search for inborn errors underlying new phenotypes, infectious and otherwise. The field of primary immunodeficiency is also expanding in other ways, with new therapeutic approaches, and with the care of patients in regions of the world where these diseases were unheard of less than a decade ago. The volume provides an overview of the field of medical genetics and its progress in 2011. Volume I opens with a dialog between the volume editors on the definition of "primary immunodeficiencies (PIDs)"; additional papers in this volume focus on PIDs in Latin America, Eastern and Central Europe, North Africa, Turkey, Asia, Iran, and the South Pacific--
פרטי הספר
- שנה
- 2011
- שפה
- English
- סדרה
- Annals of the New York Academy of Sciences -- v. 1238
- הוצאה
- Published by Blackwell Pub. on behalf of the New York Academy of Sciences
- מהדורות
- 2
- עמודים
- 144
- ISBN
- 9781573318495
מקור הנתונים: Wikidata
