On the 21th and 22th april the joint two day meeting of the Belgian and Dutch Societies of Human Genetics (BeSHG/NVGH) were held in Bruges. Kathleen, Mattias, Lynn, Robin and Bram attended this symposium. Lynn presented a poster about her work on the rare genetic disease Seckel syndrome and Robin was selected for a talk about 'BRCA testing to identify patients eligble for PARPi treatments across different indications'.
The previous day, the 20th of April, the BeSHG/NVHG organised a Genetic Retreat Symposium specifically for young PhD's to train their presentation and networking skills. We compliment the organisation for this initiative. Nele, Elyne, Sophie and Lynn attanded. Lynn presented her work entitled 'ATRIP-deficient patient expands molecular and clinical spectrum of Seckel syndrome' in a fantastic short talk.
Your comment will be posted after it is approved.
Leave a Reply.