DOI: 10.1055/s-00029030

Journal of Pediatric Neurology

Referenz

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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