Genetic testing for familial hypertrophic cardiomyopathy in newborn infants.

Lignende værker

• Identification of a mutation in the beta cardiac myosin heavy chain gene in a family with hypertrophic cardiomyopathy.
  af: al-Mahdawi, S, et al.
  Udgivet: (1993)
• An Ethical Debate: Genetic testing for familial hypertrophic cardiomyopathy in newborn infants: Testing may be unhelpful
  af: Harper, Peter S, et al.
  Udgivet: (1995)
• Genetic testing for familial hypertrophic cardiomyopathy in newborn infants. Hypertrophic cardiomyopathy can be treated but not cured.
  af: Goodwin, J. F.
  Udgivet: (1995)
• An Ethical Debate: Genetic testing for familial hypertrophic cardiomyopathy in newborn infants: Knowledge of risk allows adaptation
  af: Grigg, Leanne
  Udgivet: (1995)
• The electrocardiogram is a more sensitive indicator than echocardiography of hypertrophic cardiomyopathy in families with a mutation in the MYH7 gene.
  af: al-Mahdawi, S, et al.
  Udgivet: (1994)