Molecular characterization of tetralogy of fallot within DiGeorge critical region of the chromosome 22

Pediatric Cardiology

Volumn 22, Issue 4, 2001, Pages 279-284

  Lu, J H ^a   Chung, M Y ^a   Betau, H ^a   Chien, H P ^a   Lu, J K ^b  

^a NATIONAL YANG MING UNIVERSITY   (Taiwan)

^b NATIONAL TAIWAN OCEAN UNIVERSITY   (Taiwan)

Author keywords

Chromosome 22q11 microdeletion; DiGeorge velocardiofacial syndrome; Tetralogy of Fallot

Indexed keywords

ADOLESCENT; ARTICLE; CHILD; CHROMOSOME 22; DIGEORGE SYNDROME; EXON; FALLOT TETRALOGY; FEMALE; GENE DELETION; GENE LOCUS; HEREDITY; HETEROZYGOSITY; HUMAN; INFANT; MAJOR CLINICAL STUDY; MALE; NEWBORN; PHENOTYPE; POLYMERASE CHAIN REACTION; TANDEM REPEAT; VELOCARDIOFACIAL SYNDROME;

EID: 0034967841     PISSN: 01720643     EISSN: None     Source Type: Journal    
DOI: 10.1007/s002460010230     Document Type: Article

References (21)

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3. Congenital heart disease
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7. Comparison of occurrence of genetic syndromes in ventricular septal defect with pulmonic stenosis (classic tetralogy of Fallot) versus ventricular septal defect with pulmonic atresia
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12. Neural crest and cardiovascular patterning
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14. Interstitial 22q11 microdeletion excluding the ADU breakpoint in a patient with DiGeorge syndrome
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17. Detection of an atypical 22q11 deletion that has no overlap with the DiGeorge syndrome critical region
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21. Cardiac malformations in the velocardiofacial syndrome