Conotruncal variations in the normal heart
β Scribed by Vijaya M. Nayak; Solomon Victor
- Book ID
- 117749623
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- English
- Weight
- 129 KB
- Volume
- 7
- Category
- Article
- ISSN
- 1328-0163
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π SIMILAR VOLUMES
## Abstract ## BACKGROUND Some patients with conotruncal heart defects (CTDs) have a chromosome 22q11.2 deletion, but we do not know whether patients with CTDs who are missing the peripheral bloodβcell chromosome 22q11.2 deletion are also missing the 22q11.2 deletion in myocardial cells, and wheth
In this population-based casecontrol study, we explored the association of selected parental and infant characteristics from the birth certificates of children with conotruncal heart defects. We compared 252 cases too random sample of 5,000 nonmalformed infants from a cohort of 341,839 California li
## Abstract **INTRODUCTION:** Congenital heart defects (CHDs) are the most common structural birth defects, yet their etiology is poorly understood. As there is heterogeneity within the group of CHDs, epidemiologic studies often focus on subgroups, of conditions, such as conotruncal heart defects (