Presenting symptoms in adults with the 22q11 deletion syndrome

European Journal of Medical Genetics

Volumn 57, Issue 4, 2014, Pages 157-162

  Vogels, Annick ^a   Schevenels, Sara ^b   Cayenberghs, Richard ^c   Weyts, Eddy ^c   Van Buggenhout, Griet ^a   Swillen, Ann ^a   Van Esch, Hilde ^a   de Ravel, Thomy ^a   Corveleyn, Pieter ^b   Devriendt, Koen ^a  

^a UNIVERSITY OF LEUVEN   (Belgium)

^b UNIVERSITY HOSPITALS LEUVEN   (Belgium)

^c Sint Kamillusziekenhuis ^*  (Belgium)

Author keywords

22q11 deletion syndrome; Adults; Age at diagnosis; Intellectual disability; Presenting symptoms; Psychiatry

Indexed keywords

ADULT; ARTICLE; CHROMOSOME DELETION 22Q11; CLEFT PALATE; CLINICAL FEATURE; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL HEART MALFORMATION; DISEASE SEVERITY; FACE DYSMORPHIA; FAMILIAL DISEASE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; INTELLECTUAL IMPAIRMENT; MAJOR CLINICAL STUDY; MALE; MENTAL DISEASE; MOLECULAR DIAGNOSIS; SYMPTOMATOLOGY; 22Q11 DELETION SYNDROME; ADOLESCENT; FACE; GENETICS; MIDDLE AGED; MULTIPLE MALFORMATION SYNDROME; PALATE; PSYCHOSIS; RETROSPECTIVE STUDY; YOUNG ADULT;

22Q11 DELETION SYNDROME; ABNORMALITIES, MULTIPLE; ADOLESCENT; ADULT; COMPARATIVE GENOMIC HYBRIDIZATION; FACE; FEMALE; HEART DEFECTS, CONGENITAL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INTELLECTUAL DISABILITY; MALE; MIDDLE AGED; PALATE; PSYCHOTIC DISORDERS; RETROSPECTIVE STUDIES; YOUNG ADULT;

EID: 84898405686     PISSN: 17697212     EISSN: 18780849     Source Type: Journal    
DOI: 10.1016/j.ejmg.2014.02.008     Document Type: Article

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