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Disease-related gene duplications: more common than expected?
Guy Froyen, Human Genome Laboratory, Flanders Interuniversity institute for Biotechnology (VIB4), Dept. Human Genetics, University of Leuve, Belgium
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High throughput detection of relevant copy number variation in the human genome for association studies
Dr Benjamin Rodríguez-Santiago, Unitat de Genčtica, Universitat Pompeu Fabra, Spain
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Review of Chromosome aberration breakpoints in the context of ECARUCA (European Cytogeneticists Association Register of Unbalanced Chromosome Aberrations) Project
Dr rer nat Mariluce Riegel, Institute of Medical Genetics, University of Zurich, Switzerland
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Towards a genotype-phenotype correlation of small supernumerary marker chromosomes (sSMC)
Thomas Liehr, nstitute of Human Genetics and Anthropology, Friedrich Schiller University Jena, Germany
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Genetic variation affects de novo translocation frequencies
Mr Takema Kato, Div. Mol. Genet., ICMS, Fujita Health Univ., Japan
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Variant translocation in CML – Is it really the same as the typical translocation?
Min Fang, University of Connecticut Health Center, United States
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EWS-CREB1: A recurrent variant fusion in clear cell sarcoma associated with gastrointestinal location and absence of melanocytic differntiation
Paola Dal Cin, Brigham and Women's Hospital, Boston, MA, United States
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