Prenatal prevalence and postnatal manifestations of 16p11.2 deletions: A new insights into neurodevelopmental disorders based on clinical investigations combined with multi-omics analysis
Lan Liu, Jiamin Wang, Xijing Liu, Jing Wang, Lin Chen, Hongmei Zhu, Jingqun Mai, Ting Hu, Shanling Liu
Topics & Concepts
Copy-number variationExome sequencingSanger sequencingAutismPrenatal diagnosisGeneticsIntellectual disabilityBiologyPhenotypeMedicineBioinformaticsFetusPregnancyGeneMutationGenomePsychiatryGenomic variations and chromosomal abnormalitiesCongenital heart defects researchGenomics and Rare Diseases