Associated Papers
Functional analysis of MEIS2 splice site variant c.438 + 1G>T in a congenital heart patient.
Xu C et al.
Frontiers in Genetics, 2025
Cleft palate, congenital heart disease, and developmental delay involving MEIS2 heterozygous mutations found in the patient with attention deficit hyperactivity disorder: a case report.
Shen F et al.
Frontiers in Pediatrics, 2024
De novo missense variants in MEIS2 recapitulate the microdeletion phenotype of cardiac and palate abnormalities, developmental delay, intellectual disability and dysmorphic features.
Douglas G et al.
American Journal of Medical Genetics. Part A, 2018
36th Annual David W. Smith Workshop on Malformations and Morphogenesis: Abstracts of the 2015 annual meeting.
Gripp KW et al.
American Journal of Medical Genetics. Part A, 2016
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