Prenatal diagnosis of rearrangements in the fetal 22q11.2 region

22q11.2 deletion syndrome (22q11.2DS) and 22q11.2 duplication syndrome (22q11.2DupS) are the most common copy number variations in humans. The clinical phenotypes of these two syndromes are variable, and there...

Source: Molecular Cytogenetics - July 8, 2020 Category: Molecular Biology Authors: Suping Li, Yuxia Jin, Jing Yang, Li Yang, Ping Tang, Chiyan Zhou, Liping Wu, Jinhua Dong, Jie Chen and Huaxiang Shen Tags: Research Source Type: research