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European Journal of Human Genetics : EJHG|July 1, 1997
Refined subchromosomal location of 21 expressed sequence tags from unknown genes at region 11p15C Schwienbacher, S Sabbioni, G Barbanti-Brodano, et al.FEBS Letters|July 31, 1998
Differential actin organization by vinculin isoforms: implications for cell type-specific microfilament anchorageM Rüdiger, N Korneeva, C Schwienbacher, et al.Human Molecular Genetics|May 1, 1993
In-frame deletion of von Willebrand factor A domains in a dominant type of von Willebrand diseaseF Bernardi, P Patracchini, D Gemmati, et al.British Journal of Haematology|February 1, 1989
A recurrent missense mutation (Arg----Gln) and a partial deletion in factor VIII gene causing severe haemophilia AF Bernardi, S Volinia, P Patracchini, et al.British Journal of Haematology|May 1, 1991
Characterization of the pseudogenic and genic homologous regions of von Willebrand factorG Marchetti, P Patracchini, S Volinia, et al.Cancer Research|April 5, 2000
Abnormal RNA expression of 11p15 imprinted genes and kidney developmental genes in Wilms' tumorC Schwienbacher, A Angioni, R Scelfo, et al.Proceedings of the National Academy of Sciences of the United States of America|April 26, 2000
Gain of imprinting at chromosome 11p15: A pathogenetic mechanism identified in human hepatocarcinomasC Schwienbacher, L Gramantieri, R Scelfo, et al.Proceedings of the National Academy of Sciences of the United States of America|May 9, 1998
Transcriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samplesC Schwienbacher, S Sabbioni, M Campi, et al.Pageof 2