A 5.3Mb deletion in chromosome 18q12.3 as the smallest region of overlap in two patients with expressive speech delay

European Journal of Medical Genetics

Volumn 54, Issue 2, 2011, Pages 194-197

  Bouquillon, Sonia ^a   Andrieux, Joris ^a   Landais, Emilie ^a   Duban Bedu, Bénédicte ^a   Boidein, Françoise ^a   Lenne, Bruno ^a   Vallée, Louis ^a   Leal, Teresinha ^a   Doco Fenzy, Martine ^a   Delobel, Bruno ^a  

^a LILLE UNIVERSITY HOSPITAL   (France)

Author keywords

18q12.3; Array CGH; Expressive dysphasia; Interstitial deletion; Speech delay

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHILD; CHROMOSOME 18Q; CHROMOSOME 18Q12.3 DELETION; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; DEVELOPMENTAL DISORDER; DNA MICROARRAY; DYSPHASIA; DYSPRAXIA; FECES INCONTINENCE; FEMALE; HUMAN; HUMAN CELL; HYPERACTIVITY; IMPULSIVENESS; LYMPHOCYTE; MALE; MENTAL DEFICIENCY; PRESCHOOL CHILD; PSYCHOMETRY; SPEECH ANALYSIS;

CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 18; FEMALE; HUMANS; LANGUAGE DEVELOPMENT DISORDERS; MALE; NERVE TISSUE PROTEINS; SYNAPTOTAGMINS; YOUNG ADULT;

EID: 79952488837     PISSN: 17697212     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejmg.2010.11.009     Document Type: Article

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