Associated Papers
Diagnostic Yield of Trio Whole-Genome Sequencing in Children with Undiagnosed Developmental Delay or Congenital Anomaly: A Prospective Cohort Study.
Kim J et al.
Diagnostics (basel, Switzerland), 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
Severe childhood speech disorder: Gene discovery highlights transcriptional dysregulation.
Hildebrand MS et al.
Neurology, 2020
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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