TY  - JOUR
AU  - Cortés-Martín, Jonathan
AU  - Peñuela, Nuria López
AU  - Sánchez-García, Juan Carlos
AU  - Montiel-Troya, Maria
AU  - Díaz-Rodríguez, Lourdes
AU  - Rodríguez-Blanque, Raquel
PY  - 2022
DO  - 10.3390/children9081168
SN  - 2227-9067
UR  - http://hdl.handle.net/10668/20947
T2  - Children (Basel, Switzerland)
AB  - 22q11.2 deletion syndrome (DS 22q11.2) is a rare disease of genetic origin, caused by the loss of the q11.2 region of chromosome 22. It affects one in 4000 live newborns, and among the clinical manifestations that can occur in this syndrome are...
LA  - en
KW  - 22q11.2 deletion syndrome
KW  - DiGeorge syndrome
KW  - congenital anomalies
KW  - daily activities
KW  - rare disease
KW  - velocardiofacial syndrome
TI  - Deletion Syndrome 22q11.2: A Systematic Review.
TY  - research article
VL  - 9
ER  -