Associated Papers
Exome Sequencing Studies in Syndromic Patients With Cleft Lip and/or Palate: Systematic Review.
Cárdenas-Nieto D et al.
The Cleft Palate-craniofacial Journal : Official Publication of the American Cleft Palate-craniofacial Association, 2025
Functional analysis of MEIS2 splice site variant c.438 + 1G>T in a congenital heart patient.
Xu C et al.
Frontiers in Genetics, 2025
Human Genetics of Ventricular Septal Defect.
Perrot A et al.
Advances in Experimental Medicine and Biology, 2024
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
Success and Pitfalls of Genetic Testing in Undiagnosed Diseases: Whole Exome Sequencing and Beyond.
Barili V et al.
Genes, 2023
Intellectual disability associated with craniofacial dysmorphism, cleft palate, and congenital heart defect due to a de novo MEIS2 mutation: A clinical longitudinal study.
Gangfuß A et al.
American Journal of Medical Genetics. Part A, 2021
Heterozygous loss-of-function variants of MEIS2 cause a triad of palatal defects, congenital heart defects, and intellectual disability.
Verheije R et al.
European Journal of Human Genetics : Ejhg, 2019
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