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Human Reproduction 2008 23(11):2391; doi:10.1093/humrep/den383
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© The Author 2008. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Editor's Choice

André Van Steirteghem, Editor-in-Chief

vansteirteghema@humanreproduction.co.uk

The first 10% of the full text of this article appears below.

Mitochondrial DNA (mtDNA) mutations are the cause of rare but severe disorders, without any effective treatment. Preventing their transmission is, therefore, considered to be of key importance. Because of the complexity of mitochondrial genetics, conventional prenatal diagnosis is not a satisfactory method of genetic testing. In an Opinion article (p. 2392), the pros and cons of introducing . . . [Full Text of this Article]


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