Molecular analysis of syndromic congenital heart disease using short tandem repeat markers and semiquantitative polymerase chain reaction method

Pediatrics International

Volumn 44, Issue 3, 2002, Pages 264-268

  Shi, Yi Ru ^a   Hsieh, Kai Sheng ^b   Wu, Jer Yuarn ^a   Lee, Cheng Chun ^a   Tsai, Chang Hai ^a   Tsai, Fuu Jen ^a  

^a CHINA MEDICAL UNIVERSITY HOSPITAL   (Taiwan)

^b KAOHSIUNG VETERANS GENERAL HOSPITAL   (Taiwan)

Author keywords

Chromosome 22q11.2 deletion; DiGeorge syndrome; Semiquantitative polymerase chain reaction method; Velo cardiofacial syndrome

Indexed keywords

ACCURACY; ALLELE; ARTICLE; CHROMOSOME 22Q; CHROMOSOME DELETION; CLINICAL ARTICLE; CONTROLLED STUDY; DIGEORGE SYNDROME; DISEASE SEVERITY; GENOTYPE; HAPLOTYPE; HUMAN; MOLECULAR BIOLOGY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROMOTER REGION; TANDEM REPEAT; VELOCARDIOFACIAL SYNDROME;

CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; CRANIOFACIAL ABNORMALITIES; DIGEORGE SYNDROME; HEART DEFECTS, CONGENITAL; HUMANS; MINISATELLITE REPEATS; POLYMERASE CHAIN REACTION; TANDEM REPEAT SEQUENCES;

EID: 0036315456     PISSN: 13288067     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1442-200X.2002.01553.x     Document Type: Article

References (12)

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11. Cytogenetic findings in a prospective series of patients with DiGeorge anomaly
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