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 - 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