MEIS2 involvement in cardiac development, cleft palate, and intellectual disability

American Journal of Medical Genetics, Part A

Volumn 167, Issue 5, 2015, Pages 1142-1146

  Louw, Jacoba J ^a   Corveleyn, Anniek ^a   Jia, Yaojuan ^a   Hens, Greet ^a   Gewillig, Marc ^a   Devriendt, Koenraad ^a  

^a UNIVERSITY HOSPITALS LEUVEN   (Belgium)

Author keywords

Cardiopathy; Cleft lip; Cleft palate; Heart; Intellectual disability; Next generation sequencing (NGS)

Indexed keywords

ARGININE; HOMEODOMAIN PROTEIN; MEIS2 PROTEIN, HUMAN; TRANSCRIPTION FACTOR;

AORTA COARCTATION; ARTICLE; AUTISM; CASE REPORT; CLEFT PALATE; DISEASE SEVERITY; EXOME; FACE DYSMORPHIA; FEEDING DISORDER; FEMALE; GENE; GENE DELETION; GENOTYPE PHENOTYPE CORRELATION; HEART DEVELOPMENT; HEART VENTRICLE SEPTUM DEFECT; HUMAN; INTELLECTUAL IMPAIRMENT; MEIS2 GENE; MOTOR DEVELOPMENT; MUTATIONAL ANALYSIS; PALPEBRAL FISSURE; PRIORITY JOURNAL; SCORING SYSTEM; SEQUENCE ANALYSIS; SYNDACTYLY; CHROMOSOME DELETION; DNA SEQUENCE; GENETICS; GROWTH, DEVELOPMENT AND AGING; HEART; HEART SEPTUM DEFECT; MUTATION; PATHOPHYSIOLOGY; PRESCHOOL CHILD;

CHILD, PRESCHOOL; CHROMOSOME DELETION; CLEFT PALATE; EXOME; FEMALE; HEART; HEART SEPTAL DEFECTS; HOMEODOMAIN PROTEINS; HUMANS; INTELLECTUAL DISABILITY; MUTATION; SEQUENCE ANALYSIS, DNA; TRANSCRIPTION FACTORS;

EID: 84927912279     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.36989     Document Type: Article

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