Frequency of 22q11.2 microdeletion in sporadic non-syndromic tetralogy of Fallot cases

International Journal of Cardiology

Volumn 126, Issue 3, 2008, Pages 374-378

  Gioli Pereira, L ^a   Pereira, A C ^a   Bergara, D ^a   Mesquita, S ^a   Lopes, A A ^a   Krieger, J E ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

Congenital heart disease; del22q11; Human; Mutation

Indexed keywords

ADOLESCENT; ARTICLE; CHILD; CHROMOSOME 22Q; CHROMOSOME DELETION; CONTROLLED STUDY; DNA EXTRACTION; FALLOT TETRALOGY; FEMALE; GENOTYPE PHENOTYPE CORRELATION; HOMOZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MALE; MEDICAL RECORD REVIEW; PHYSICAL EXAMINATION; PREVALENCE; PRIORITY JOURNAL; PULMONARY VALVE ATRESIA; PULMONARY VALVE STENOSIS; SINGLE NUCLEOTIDE POLYMORPHISM; VENOUS BLOOD;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; COHORT STUDIES; FEMALE; FOLLOW-UP STUDIES; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; INCIDENCE; MALE; PROBABILITY; RETROSPECTIVE STUDIES; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RISK ASSESSMENT; SEVERITY OF ILLNESS INDEX; TETRALOGY OF FALLOT;

EID: 43049183037     PISSN: 01675273     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijcard.2007.04.043     Document Type: Article

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