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  • Isolated imprinting mutation of the DLK1/GTL2 locus associated with a clinical presentation of maternal uniparental disomy of chromosome 14

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Findings that shed new light on the possible pathogenesis of a disease or an adverse effect
Isolated imprinting mutation of the DLK1/GTL2 locus associated with a clinical presentation of maternal uniparental disomy of chromosome 14
  1. I K Temple1,2,
  2. V Shrubb3,
  3. M Lever4,
  4. H Bullman4,
  5. D J G Mackay1,4
  1. 1
    Division of Human Genetics, University of Southampton, Southampton, Hampshire, UK
  2. 2
    Wessex Genetics Service, Southampton University Hospitals Trust, Southampton, Hampshire, UK
  3. 3
    Department of Community Child Health, Southampton Community Trust, Southampton, Hampshire, UK
  4. 4
    Wessex Regional Genetics Laboratory, Salisbury Health Care Trust, Salisbury, Hampshire, UK
  1. I K Temple, ikt{at}soton.ac.uk

Footnotes

  • Competing interests: none.

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http://dx.doi.org/10.1136/bcr.06.2009.1997

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    Footnotes

    • Competing interests: none.

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