Chromosome 22q11 microdeletion and congenital heart disease - A survey in a paediatric population

European Journal of Pediatrics

Volumn 158, Issue 7, 1999, Pages 566-570

  Yong, D E J ^b   Booth, P ^b   Baruni, J ^a   Massie, D ^a   Stephen, G ^a   Couzin, D ^a   Dean, J C S ^a  

^a UNIVERSITY OF ABERDEEN   (United Kingdom)

^b NONE

Author keywords

CATCH 22; Congenital heart disease; Microdeletion chromosome 22q11

Indexed keywords

ARTICLE; CHROMOSOME 22Q; CHROMOSOME DELETION; CONGENITAL HEART DISEASE; CONTROLLED STUDY; DIGEORGE SYNDROME; FAMILY STUDY; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC LINKAGE; HUMAN; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; SYNDROME CHARGE;

CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DATA COLLECTION; FEMALE; FOLLOW-UP STUDIES; GREAT BRITAIN; HEART DEFECTS, CONGENITAL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INCIDENCE; INFANT; INFANT, NEWBORN; MALE; PEDIGREE; RISK ASSESSMENT; SENSITIVITY AND SPECIFICITY;

EID: 0032998472     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004310051148     Document Type: Article

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