10th Annual meeting of the Belgian Society for Human Genetics:The Dark Side of the Genome.

Related content

• Research output

• Replacement of FISH by genome-wide single cell array analysis for preimplantation genetic diagnosis of translocation carriers

  Research output: Contribution to journal › Editorial

• Mutation analysis of the NEMO gene in patients with Incontinentia Pigmenti

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

• Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to the m.14487T>C mutation in ND6.

  Research output: Contribution to journal › Meeting abstract (Journal)

• Progressieve myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to m.14487T>C in ND6

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

• Molecular spectrum of androgen receptor gene alterations in Belgian patients

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

• Are defects in meiosis genes involved in recurrent pregnancy loss rather than in male infertility?

  Research output: Contribution to journal › Editorial

• Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to m.14487T>C

  Research output: Contribution to journal › Article › peer-review

• Projects

• Molecular investigations in the patients with defects in the complexes of the oxidative phosphorylation and the pyruvate dehydrogenase complex.

  Project: Fundamental