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M Erdel

Showing results (31-40 of 36) with videos related to

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Clinical Genetics|January 6, 2007
Two novel translocation breakpoints upstream of SOX9 define borders of the proximal and distal breakpoint cluster region in campomelic dysplasiaM Leipoldt, M Erdel, G A Bien-Willner, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|May 15, 2010
Clinical outcome of pretreated B-cell chronic lymphocytic leukemia following alemtuzumab therapy: a retrospective study on various cytogenetic risk categoriesM Fiegl, M Erdel, I Tinhofer, et al.
Gene|May 16, 1998
Characterization of the human gene coding for the swelling-dependent chloride channel ICln at position 11q13.5-14.1 (CLNS1A) and further characterization of the chromosome 6 (CLNS1B) localizationU O Nagl, M Erdel, F Bergmann, et al.
Oncogene|April 26, 2011
Regulation of transcription factor E2F3a and its clinical relevance in ovarian cancerD Reimer, M Hubalek, H Kiefel, et al.
Clinical Genetics|June 30, 2010
Parental origin of apparently balanced de novo complex chromosomal rearrangements investigated by microdissection, whole genome amplification, and microsatellite-mediated haplotype analysisV Grossmann, M Höckner, H Karmous-Benailly, et al.
European Journal of Human Genetics : EJHG|March 27, 1999
Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndromeA Silahtaroglu, F A Hol, P K Jensen, et al.
Pageof 4

Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
Clinical Genetics|January 6, 2007
Two novel translocation breakpoints upstream of SOX9 define borders of the proximal and distal breakpoint cluster region in campomelic dysplasiaM Leipoldt, M Erdel, G A Bien-Willner, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|May 15, 2010
Clinical outcome of pretreated B-cell chronic lymphocytic leukemia following alemtuzumab therapy: a retrospective study on various cytogenetic risk categoriesM Fiegl, M Erdel, I Tinhofer, et al.
Gene|May 16, 1998
Characterization of the human gene coding for the swelling-dependent chloride channel ICln at position 11q13.5-14.1 (CLNS1A) and further characterization of the chromosome 6 (CLNS1B) localizationU O Nagl, M Erdel, F Bergmann, et al.
Oncogene|April 26, 2011
Regulation of transcription factor E2F3a and its clinical relevance in ovarian cancerD Reimer, M Hubalek, H Kiefel, et al.
Clinical Genetics|June 30, 2010
Parental origin of apparently balanced de novo complex chromosomal rearrangements investigated by microdissection, whole genome amplification, and microsatellite-mediated haplotype analysisV Grossmann, M Höckner, H Karmous-Benailly, et al.
European Journal of Human Genetics : EJHG|March 27, 1999
Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndromeA Silahtaroglu, F A Hol, P K Jensen, et al.
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