De novo missense variants in MEIS2 recapitulate the microdeletion phenotype of cardiac and palate abnormalities, developmental delay, intellectual disability and dysmorphic features

American Journal of Medical Genetics Part A, EarlyView.

Source: American Journal of Medical Genetics Part A - July 28, 2018 Category: Genetics & Stem Cells Authors: Ganka Douglas , Megan T. Cho , Aida Telegrafi , Susan Winter , Jason Carmichael , Elaine H. Zackai , Matthew A. Deardorff , Margaret Harr , Linford Williams , Apostolos Psychogios , Angelika L. Erwin , Theresa G Source Type: research