De novo deletion of FMN2 in a girl with mild non-syndromic intellectual disability

European Journal of Medical Genetics

Volumn 56, Issue 12, 2013, Pages 686-688

  Almuqbil, Mohammed ^a   Hamdan, Fadi F ^b   Mathonnet, Géraldine ^b   Rosenblatt, Bernard ^a   Srour, Myriam ^a  

^a MONTREAL CHILDREN S HOSPITAL   (Canada)

^b UNIVERSITY OF MONTREAL   (Canada)

Author keywords

Chromosome 1q43; FMN2; FORMIN 2; Intellectual disability

Indexed keywords

FORMIN 2; PEPTIDES AND PROTEINS; UNCLASSIFIED DRUG;

ARTICLE; CASE REPORT; CHILD; COMPARATIVE GENOMIC HYBRIDIZATION; ELECTROENCEPHALOGRAM; FAMILY HISTORY; FEMALE; FMN2 GENE; GENE; GENE DELETION; HETEROZYGOSITY; HUMAN; INTELLECTUAL IMPAIRMENT; MEDICAL HISTORY; NEUROPSYCHOLOGY; SCHOOL CHILD;

CHROMOSOME 1Q43; FMN2; FORMIN-2; INTELLECTUAL DISABILITY;

CHILD; FEMALE; GENE DELETION; HETEROZYGOTE; HUMANS; INTELLECTUAL DISABILITY; MICROFILAMENT PROTEINS; NUCLEAR PROTEINS;

EID: 84888019403     PISSN: 17697212     EISSN: 18780849     Source Type: Journal    
DOI: 10.1016/j.ejmg.2013.10.003     Document Type: Article

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