11th International Congress of Human Genetics

Session Details

More Than Rare Syndromes

Thursday, 10 August 2006 11:00 -13:00

Great Hall

Co-Chair Georgia Chenevix-Trench Queensland Institute of Medical ResearchAustralia
Co-Chair Graeme Suthers Women's & Children's HospitalAustralia

Generation of an ATM knock in mouse with the breast-cancer susceptibility mutation, 7271T>G
  • Dr Jeremy Arnold, Queensland Institute of Medical Research, Australia
  • Increased cancer risk of heterozygotes with NBS1 founder mutation
  • Prof Karl Sperling, Institute of Human Genetics, Charité - Universitätsmedizin Berlin, Germany
  • Nijmegen Breakage Syndrome: hypomorphic mutation, protein expression and phenotypic variability
  • Martin Digweed, Institut für Humangenetik, Charité - Universitätsmedizin Berlin., Germany
  • LKB1 tumor suppressor gene alterations in sporadic lung adenocarcinomas
  • Montserrat Sanchez-Cespedes, Spanish National Cancer Centre, Spain
  • Prostate Specific Antigen(PSA) gene polymorphism and its Interaction with Androgen Receptor Trinucleotide Repeats (CAG) in Prostate Cancer
  • Dr Rama Devi Mittal, Sanjay Gandhi Post Graduate Institute of Medical Sciences, India
  • Evidence for a broader role of the tumor suppressor BRCA1 at specific genomic sites during their replication
  • Gayle J Pageau, University of Massachusetts Medical School, United States
  • Telomere-mediated genomic instability in breast tumour cells and in cells from mice lacking breast cancer genes
  • Dr Prakash Hande, Department of Physiology, Yong Loo Lin School of Medicine, National University of Singapore
  • Genetic mapping in Trp53+/- mice identifies DMBT1 as a potential modifier of breast cancer risk
  • Dr Anneke C Blackburn, Australian National University, Canberra ACT, Australia
  • Published on Tuesday, 1 August 2006 by the Professional Conference Organiser