𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Genetic analyses in two extended families with deletion 22q11 syndrome: Importance of extracardiac manifestations

✍ Scribed by Kerry A. Shooner; Alan F. Rope; Robert J. Hopkin; Gregor U. Andelfinger; D. Woodrow Benson


Book ID
116683101
Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
176 KB
Volume
146
Category
Article
ISSN
1097-6833

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Idiopathic thrombocytopenic purpura in t
✍ LΓ©vy, A.; Michel, G.; Lemerrer, M.; Philip, N. πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 165 KB πŸ‘ 1 views

The phenotypic spectrum caused by the microdeletion of chromosome 22q11 region is known to be variable. Nearly all patients with DiGeorge sequence (DGS) and approximately 60% of patients with velocardiofacial syndrome exhibit the deletion. Recent papers have reported various congenital defects in pa