Open AccessPrenatal diagnosis and molecular cytogenetic characterization of an inherited microdeletion of chromosome 16p11.2
Author(s) -
Meihua Li,
Linlin Liu,
Yijun Wu,
Jian Guan
Publication year - 2022
Publication title -
journal of international medical research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.421
H-Index - 57
eISSN - 1473-2300
pISSN - 0300-0605
DOI - 10.1177/03000605221109400
Subject(s) - genetic counseling , copy number variation , microdeletion syndrome , prenatal diagnosis , medicine , genetics , karyotype , autism , chromosome , microarray , autism spectrum disorder , biology , fetus , gene , pregnancy , genome , psychiatry , gene expression