DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Auber B, Burfeind P, Herold S. et al.
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.
Clin Genet 2007;
72 (05) 454-459
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