TBX1 gene mutation screening in patients with non-syndromic Fallot tetralogy

Turkish Journal of Pediatrics

Volumn 49, Issue 1, 2007, Pages 61-68

  Çabuk, Feryal ^a   Karabulut, Halil G ^b   Tuncali, Timur ^b   Karademir, Selmin ^a   Bozdayi, Mithat ^b   Tükün, Ajlan ^b  

^a DR SAMI ULUS CHILDREN S HOSPITAL   (Turkey)

^b ANKARA UNIVERSITY   (Turkey)

Author keywords

Conotruncal cardiac anomaly; TBX1; Tetralogy of Fallot

Indexed keywords

T BOX TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR TBX1; UNCLASSIFIED DRUG;

ALLELE; ARTICLE; CHILD; CHROMOSOME 22Q; CHROMOSOME DELETION; CLINICAL ARTICLE; CONTROLLED STUDY; EXON; FALLOT TETRALOGY; FEMALE; GENE MUTATION; GENETIC SCREENING; GENOTYPE PHENOTYPE CORRELATION; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; INFANT; MALE; VOLUNTEER;

CHILD; CHILD, PRESCHOOL; FEMALE; GENETIC SCREENING; HUMANS; INFANT; INFANT, NEWBORN; MALE; MUTATION; NEURAL CREST; POLYMERASE CHAIN REACTION; T-BOX DOMAIN PROTEINS; TETRALOGY OF FALLOT;

EID: 34247142485     PISSN: 00414301     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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