A new patient with a terminal de novo 2p25.3 deletion of 1.9 Mb associated with early-onset of obesity, intellectual disabilities and hyperkinetic disorder

Molecular Cytogenetics

Volumn 7, Issue 1, 2014, Pages

  Bonaglia, Maria Clara ^a   Giorda, Roberto ^a   Zanini, Sergio ^a  

^a SCIENTIFIC INSTITUTE   (Italy)

Author keywords

Deletion 2p25.3; Hypekinetic disorder; Language delay; MYT1L; Obesity

Indexed keywords

MYELIN TRANSCRIPTION FACTOR 1; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

ARTICLE; CASE REPORT; CHILD; CHILD DEVELOPMENT; CHROMOSOME DELETION; CHROMOSOME DELETION 2P25.3; COMPARATIVE GENOMIC HYBRIDIZATION; ELECTROCARDIOGRAM; ELECTROENCEPHALOGRAM; FEMALE; GENOTYPE; HAPLOINSUFFICIENCY; HUMAN; HYPERKINESIA; INTELLECTUAL IMPAIRMENT; MONOSOMY; NUCLEAR MAGNETIC RESONANCE IMAGING; OBESITY; PHENOTYPE; POLYMORPHIC LOCUS; PRESCHOOL CHILD;

EID: 84906549240     PISSN: None     EISSN: 17558166     Source Type: Journal    
DOI: 10.1186/1755-8166-7-53     Document Type: Article

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