Concurrent Sessions
Tuesday, May 9, 2006, 10.45 - 12.15 hrs - Forum
C11. Clinical and molecular cytogenetics
C64. Distinctive white matter abnormalities on MRI in patients with 6p deletion syndrome
S. A. J. Lesnik Oberstein1, M. Kriek1,
K. Szuhai2, A. van Haeringen1, J. van der Smagt3,
K. B. M. Hansson1, M. H. Breuning1, M. S. van der Knaap4;
1Center for Human and Clinical Genetics, Leiden University Medical
Center, Leiden, The Netherlands, 2Department of Molecular Cell
Biology, Leiden University Medical Center, Leiden, The Netherlands, 3Department
of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands,
4Department of child neurology, VUMC, Amsterdam, The Netherlands.
C65. Array-CGH: A novel tool in genetic diagnosis of
individuals with congenital heart defects
B. Thienpont1, L. Mertens2,
B. Eyskens2, D. Boshoff2, N. Maas1, T. de Ravel1,
J. Fryns1, M. Gewillig2, J. R. Vermeesch1, K.
Devriendt1;
1Center for Human Genetics, Leuven, Belgium, 2Pediatric
Cardiology Unit, Leuven, Belgium.
C66. Molecular cytogenetic (re-)examinations of structural
chromosome aberrations within the ECARUCA (European Cytogeneticists Association
Register of Unbalanced Chromosome Aberrations) project reveals surprising
results
M. Riegel, A. Schinzel;
University of Zürich, Schwerzenbach, Switzerland.
C67. Targeted cloning of fragile sites - based on a
previous tagging of fragile regions in a breast cancer cell line
A. Fechter, E. Kuehnel, I. Buettel, L. Savelyeva,
M. Schwab;
German Cancer Research Center, Heidelberg, Germany.
C68. Genome wide tiling path array CGH analysis in a
diagnostic setting. A three-year experience
N. de Leeuw, R. Pfundt, D. Koolen, E. Sistermans,
W. Nillesen, M. Egmont-Petersen, J. Veltman, A. Geurts van Kessel, B. de Vries,
D. Smeets;
Dept. of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
C69. Subtelomeric imbalances in phenotypically normal
individuals
I. G. Balikova1, T. de Ravel1,
C. Le Caignec1, B. Thienpont1, B. Menten2, F.
Speleman2, K. Devriendt1, J. P. Fryns1, J. R.
Vermeesch1;
1Center for Human Genetics, Leuven, Belgium, 2Center for
Medical Genetics Ghent, Ghent, Belgium.