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B Auber, P Burfeind, S Herold, K Schoner, G Simson, R Rauskolb and H Rehder A disease causing deletion of 29 base pairs in intron 15 in the MKS1 gene is highly associated with the campomelic variant of the Meckel–Gruber syndrome Clinical Genetics 72

Version of Record online: 5 SEP 2007 | DOI: 10.1111/j.1399-0004.2007.00880.x

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