Congenital heart malformations: Aetiology and associations

Seminars in Neonatology

Volumn 6, Issue 1, 2001, Pages 17-25

  Brennan, Paul ^a   Young, Ian D ^a  

^a NOTTINGHAM CITY HOSPITAL   (United Kingdom)

Author keywords

Chromosomes; Congenital heart malformation; Developmental genes; Dysmorphology; Syndrome

Indexed keywords

ANEUPLOIDY; AUTOSOMAL DISORDER; CHILD; CHROMOSOME; CHROMOSOME 13; CHROMOSOME 21; CHROMOSOME 22; CHROMOSOME 22Q; CHROMOSOME 3P; CHROMOSOME 4P; CHROMOSOME 5P; CHROMOSOME 8P; CHROMOSOME 9P; CHROMOSOME DELETION; CONGENITAL HEART MALFORMATION; FETUS; GENE MUTATION; HEART VENTRICLE SEPTUM; HOMEOBOX; HUMAN; PRENATAL DRUG EXPOSURE; PRENATAL EXPOSURE; REVIEW; TRISOMY;

EID: 0035153689     PISSN: 10842756     EISSN: None     Source Type: Journal    
DOI: 10.1053/siny.2000.0032     Document Type: Article

References (14)

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13. Smith-Lemli-Opitz syndrome: A variable clinical and biochemical phenotype