B Auber

Summary

Country: Germany

Publications

  1. ncbi 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
    B Auber
    Institute of Human Genetics, University of Goettingen, Germany
    Clin Genet 72:454-9. 2007

Detail Information

Publications1

  1. ncbi 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
    B Auber
    Institute of Human Genetics, University of Goettingen, Germany
    Clin Genet 72:454-9. 2007
    ..In families with a known mutation in the MKS1 gene, it is now possible to offer an early prenatal testing, for example with chorionic villus sampling and mutation analysis...