Genetic Counseling and Prenatal Diagnosis for mtDNA Disease

This publication has 10 references indexed in Scilit:

• MELAS and MERRF. The relationship between maternal mutation load and the frequency of clinically affected offspring
  Brain, 1998
• Epidemiology of A3243G, the Mutation for Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes: Prevalence of the Mutation in an Adult Population
  American Journal of Human Genetics, 1998
• Is the Bottleneck Cracked?
  American Journal of Human Genetics, 1998
• Clinical features, investigation, and management of patients with defects of mitochondrial DNA
  Journal of Neurology, Neurosurgery & Psychiatry, 1997
• Mammalian mitochondrial genetics: heredity, heteroplasmy and disease
  Trends in Genetics, 1997
• Mitochondrial medicine
  QJM: An International Journal of Medicine, 1997
• Molecular pathology of MELAS and MERRF. The relationship between mutation load and clinical phenotypes
  Brain, 1997
• Random genetic drift in the female germline explains the rapid segregation of mammalian mitochondrial DNA
  Nature Genetics, 1996
• Mitotic activity during preimplantation development of human embryos
  Reproduction, 1995
• Mitochondrial gene segregation in mammals: is the bottleneck always narrow?
  Human Genetics, 1992