Frequency of 22q11 deletions in children with isolated conotruncal defects

Chinese Journal of Contemporary Pediatrics

Volumn 11, Issue 1, 2009, Pages 25-28

  Shen, Lei ^a   Xu, Yue Juan ^a   Zhao, Peng Jun ^a   Sun, Kun ^a  

^a SHANGHAI JIAO TONG UNIVERSITY SCHOOL OF MEDICINE   (China)

Author keywords

22q11.2; Child; Chromosome; Conotruncal anomaly; Fluorescence in situ hybridization

Indexed keywords

ADOLESCENT; ARTICLE; CARDIOVASCULAR MALFORMATION; CHILD; CHILD CARE; CHINA; CHROMOSOME 22Q; CLINICAL ARTICLE; CONGENITAL HEART DISEASE; CONGENITAL HEART MALFORMATION; CONTROLLED STUDY; FALLOT TETRALOGY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE FREQUENCY; GENETIC SCREENING; HEART RIGHT VENTRICLE DOUBLE OUTLET; HEART VENTRICLE SEPTUM DEFECT; HUMAN; INFANT; MALE; PROSPECTIVE STUDY; PULMONARY VALVE ATRESIA; RARE DISEASE; SAMPLING;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; HEART DEFECTS, CONGENITAL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; MALE;

EID: 58649122901     PISSN: 10088830     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (17)

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