Genetic characterisation of 22q11.2 variations and prevalence in patients with congenital heart disease

Hou, HT; Chen, HX; Wang, XL; Yuan, C; Yang, Q; Liu, ZG; He, GW

Liu, ZG; He, GW (corresponding author), Chinese Acad Med Sci & Peking Union Med Coll, TEDA Int Cardiovasc Hosp, Tianjin 300457, Peoples R China.

ARCHIVES OF DISEASE IN CHILDHOOD, 2020; 105 (4): 367

Abstract

Objectives The 22q11.2 deletion syndrome is considered the most frequent chromosomal microdeletion syndrome in humans and the second leading chromosom......

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