TY  - GEN 
AU  - Cortés Martín, Jonathan
AU  - Sánchez García, Juan Carlos
AU  - Montiel Troya, María
AU  - Díaz Rodríguez, Consuelo Lourdes
AU  - Rodríguez Blanque, Raquel
PY  - 2022
UR  - https://hdl.handle.net/10481/76957
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  - eng
PB  - MDPI
KW  - 22q11.2 deletion syndrome
KW  - DiGeorge syndrome
KW  - Velocardiofacial syndrome
KW  - Rare disease
KW  - Congenital anomalies
KW  - Daily activities
TI  - Deletion Syndrome 22q11.2: A Systematic Review
DO  - 10.3390/children9081168
ER  -