Long ‐term natural history of an adult patient with distal 22q11.2 deletion from low copy repeat‐D to E
Congenital Anomalies, EarlyView.
Source: Congenital Anomalies - Category: Genetics & Stem Cells Authors: Mari
Matsuo
,
Toshiyuki
Yamamoto
,
Kayoko
Saito Source Type: research
More News: Genetics | Microdeletion Syndromes