PGD and heteroplasmic mitochondrial DNA point mutations: a systematic review estimating the chance of healthy offspring

Mutational analysis of whole mitochondrial DNA in patients with MELAS and MERRF diseases

(2010) Byung-Ok Choi et al.   EXPERIMENTAL AND MOLECULAR MEDICINE

Segregation of mtDNA throughout human embryofetal development: m.3243A>G as a model system

(2010) Sophie Monnot et al.   HUMAN MUTATION

Avoiding transgenerational risks of mitochondrial DNA disorders: a morally acceptable reason for sex selection?

(2010) A. L. Bredenoord et al.   HUMAN REPRODUCTION

Cardiac involvement is frequent in patients with the m.8344A>G mutation of mitochondrial DNA

(2010) K. Wahbi et al.   NEUROLOGY

174th ENMC International Workshop: Applying pre-implantation genetic diagnosis to mtDNA diseases: Implications of scientific advances 19–21 March 2010, Naarden, The Netherlands

(2010) J. Poulton et al.   NEUROMUSCULAR DISORDERS

Transmission of Mitochondrial DNA Diseases and Ways to Prevent Them

(2010) Joanna Poulton et al.   PLoS Genetics

Preimplantation genetic diagnosis for mitochondrial DNA disorders: ethical guidance for clinical practice

(2009) Annelien Bredenoord et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Information for genetic management of mtDNA disease: sampling pathogenic mtDNA mutants in the human germline and in placenta

(2009) D. Marchington et al.   JOURNAL OF MEDICAL GENETICS

Prevalence of Mitochondrial 1555A→G Mutation in European Children

(2009) Maria Bitner-Glindzicz et al.   NEW ENGLAND JOURNAL OF MEDICINE

Prevalence of Mitochondrial 1555A→G Mutation in Adults of European Descent

(2009) Himesha Vandebona et al.   NEW ENGLAND JOURNAL OF MEDICINE

Pathogenic Mitochondrial DNA Mutations Are Common in the General Population

(2008) Hannah R. Elliott et al.   AMERICAN JOURNAL OF HUMAN GENETICS