Belgian Society for Human Genetics, 13th meeting: Genetics of Human Development EXPOsed

Related content

• Research output

• Use of next generation sequencing (NGS) in mitochondrial (mt) disorders: whole mitochondrial genome analysis

  Research output: Chapter in Book/Report/Conference proceeding › Meeting abstract (Book) › Research

• Double jeopardy : Identification of a Fragile X full mutation associated with Turner Syndrome in a prenatal case.

  Research output: Chapter in Book/Report/Conference proceeding › Meeting abstract (Book) › Research

• AmplideX FMR1 PCR kit as a substitute for the Southern blot technique to detect large CGG repeats in FMR1 gene

  Research output: Chapter in Book/Report/Conference proceeding › Meeting abstract (Book) › Research

• 15 years of Yq microdeletion analysis in UZ Brussel

  Research output: Chapter in Book/Report/Conference proceeding › Meeting abstract (Book) › Research

• Projects

• Research at the interface between human genetics and reproduction.

  Project: Fundamental

• Development of diagnostic, biochemical and molecular methods, the prevention and the study of treatment of OXPHOS deficiency.

  Project: Fundamental

• Development of diagnostic, biochemical and molecular methods, the prevention and the study of treatment of OXPHOS deficiency.

  Project: Fundamental