Complex congenital heart defects in association with maternal diabetes and partial deletion of the A2BP1 gene

Fetal and Pediatric Pathology

Volumn 30, Issue 3, 2011, Pages 161-166

  Lale, Seema ^a   Yu, Shihui ^b   Ahmed, Atif ^b  

^a UNIVERSITY OF MISSOURI KANSAS CITY   (United States)

^b CHILDREN S MERCY HOSPITAL   (United States)

Author keywords

A2BP1 gene; congenital heart defects; Maternal diabetes

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 16P; CONGENITAL HEART DISEASE; DISEASE ASSOCIATION; FEMALE; GENE DELETION; GENETIC TRANSCRIPTION; HUMAN; INFANT; MATERNAL DIABETES MELLITUS; PHENOTYPE; PRIORITY JOURNAL; SEPSIS;

ADULT; AUTOPSY; CHROMOSOMES, HUMAN, PAIR 16; FEMALE; GENE DELETION; HEART DEFECTS, CONGENITAL; HUMANS; INFANT; INFANT, NEWBORN; PREGNANCY; PREGNANCY IN DIABETICS; RNA-BINDING PROTEINS;

EID: 79955662802     PISSN: 15513815     EISSN: 15513823     Source Type: Journal    
DOI: 10.3109/15513815.2010.547555     Document Type: Article

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