Concurrent Sessions
Monday, May 7, 2006, 15.00 - 16.30 hrs - Auditorium
C05. Genetic analysis of complex disease II
C28. Loci of shared segmental aneuploidy in the genomes of
healthy and mentally retarded subjects detected by Array-CGH
M. Poot, M. J. Eleveld, R. Hochstenbach, H. K.
Ploos van Amstel;
Department Medical Genetics, 3508 AB Utrecht, The Netherlands.
C29. Distribution of recurrent copy number variations in
different ethnic populations
L. E. L. M. Vissers1, S. J. White2,
A. Geurts van Kessel1, E. Kalay1, A. E. Lehesjoki3,
P. C. Giordano2, E. van de Vosse4, M. H. Breuning2,
H. G. Brunner1, J. T. den Dunnen2, J. A. Veltman1;
1Department of Human Genetics, NCMLS, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands, 2Center for Human and
Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands,
3Folkhalsan Institute of Genetics, Neuroscience Center and Department
of Medical Genetics, University of Helsinki, Helsinki, Finland, 4Department
of Infectious Diseases, Leiden University Medical Center, Leiden, The
Netherlands.
C30. Systematic prediction of the boundaries of large copy
number variants in the human genome
J. O. Korbel1,2, A. E. Urban1,
S. M. Weissman1, M. Snyder3, M. B. Gerstein1;
1Yale University School of Medicine, New Haven, CT, United States,
2European Molecular Biology Laboratory, Heidelberg, Germany, 3Yale
University, New Haven, CT, United States.
C31. Identification of haplotypes in the human Foxo1a and
Foxo3a genes influencing disease at old age and lifespan
M. Kuningas1, S. P. Mooijaart1,
P. E. Slagboom2, R. G. J. Westendorp1, D. van Heemst1;
1Department of Gerontology and Geriatrics, Leiden University Medical
Center, Leiden, The Netherlands, 2Section of Molecular Epidemiology,
Department of Medical Statistics, Leiden University Medical Center, Leiden, The
Netherlands.
C32. Identification and Functional Analysis of CITED2
Mutations in Patients with Congenital Heart Defects
S. Hammer1, C. H. Grimm1, I. Dunkel1,
S. Mebus2, H. Sperling2, A. Ebner3, R. Galli1,
H. Lehrach1, C. Fusch3, F. Berger2, S.
Sperling1;
1Max Planck Institute for Moleculare Genetics, Berlin, Germany,
2German Heart Center Berlin, Berlin, Germany, 3Ernst-Moritz-Arndt
University, Greifswald, Germany.
C33. Mutations in Desmoglein-2 gene are associated to
arrhythmogenic right ventricular cardiomyopathy
K. Pillichou1, G. Beffagna1, A.
Nava2, C. Basso3, B. Bauce2, A. Lorenzon1,
A. Vettori1, J. Towbin4, G. Thiene3, G. A.
Danieli1, A. Rampazzo1;
1Department of Biology, Padua, Italy, 2Department of
Cardio-Thoracic-vascular Sciences, Padua, Italy, 3Institute of
Pathology, Padua, Italy, 4Department of Pediatrics, Houston, TX,
United States.