Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome. [electronic resource]
Producer: 20030718Description: 2072-6 p. digitalISSN:- 0735-1097
- Adolescent
- Adult
- Aged
- Aged, 80 and over
- Australia
- Child
- Child, Preschool
- Cohort Studies
- Family Health
- Female
- Genes, Homeobox -- genetics
- Genetic Markers -- genetics
- Heart Block -- genetics
- Heart Conduction System -- pathology
- Heart Defects, Congenital -- genetics
- Heart Septal Defects, Atrial -- genetics
- Homeobox Protein Nkx-2.5
- Homeodomain Proteins -- genetics
- Humans
- Hypoplastic Left Heart Syndrome -- genetics
- Infant
- Infant, Newborn
- Male
- Middle Aged
- Point Mutation -- genetics
- Polymorphism, Genetic -- genetics
- Retrospective Studies
- Statistics as Topic
- Transcription Factors
- United States
- Xenopus Proteins
No physical items for this record
Publication Type: Comparative Study; Evaluation Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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