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B Streubel

Showing results (1-10 of 35) with videos related to

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Cancer Genetics and Cytogenetics|February 13, 2001
Amplification of the AML1(CBFA2) gene on ring chromosomes in a patient with acute myeloid leukemia and a constitutional ring chromosome 21B Streubel, P Valent, K Lechner, et al.
Klinische Monatsblatter Fur Augenheilkunde|November 24, 2007
[Bilateral uveal melanoma: a case report]R Dunavoelgyi, I Dejaco-Ruhswurm, B Streubel, et al.
Leukemia|February 11, 2005
T(3;14)(p14.1;q32) involving IGH and FOXP1 is a novel recurrent chromosomal aberration in MALT lymphomaB Streubel, U Vinatzer, A Lamprecht, et al.
Gut|November 22, 2005
Successful antibiotic treatment of Helicobacter pylori negative gastric mucosa associated lymphoid tissue lymphomasM Raderer, B Streubel, S Wöhrer, et al.
Wiener Medizinische Wochenschrift (1946)|January 1, 1996
[In vitro transformation of amniotic cells to muscle cells--background and outlook]B Streubel, G Martucci-Ivessa, T Fleck, et al.
Leukemia|December 13, 2005
Novel t(5;9)(q33;q22) fuses ITK to SYK in unspecified peripheral T-cell lymphomaB Streubel, U Vinatzer, M Willheim, et al.
Gut|March 25, 2006
MALT lymphoma associated genetic aberrations occur at different frequencies in primary and secondary intestinal MALT lymphomasB Streubel, G Seitz, M Stolte, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|January 8, 2013
Prenatal microarray analysis as second-tier diagnostic test: single-center prospective studyM Schmid, S Stary, S Springer, et al.
Neuropediatrics|August 1, 1994
Coisogenic all-plus-one immunization: a model for identifying missing proteins in null-mutant conditions. Antibodies to dystrophin in mdx mouse after transplantation of muscle from normal coisogenic donorR E Bittner, B Streubel, S Shorny, et al.
American Journal of Medical Genetics|October 21, 1999
Somatic mosaicism of a greater than 1.7-Mb deletion of genomic DNA involving the entire NF1 gene as verified by FISH: further evidence for a contiguous gene syndrome in 17q11.2B Streubel, E Latta, H Kehrer-Sawatzki, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
Cancer Genetics and Cytogenetics|February 13, 2001
Amplification of the AML1(CBFA2) gene on ring chromosomes in a patient with acute myeloid leukemia and a constitutional ring chromosome 21B Streubel, P Valent, K Lechner, et al.
Klinische Monatsblatter Fur Augenheilkunde|November 24, 2007
[Bilateral uveal melanoma: a case report]R Dunavoelgyi, I Dejaco-Ruhswurm, B Streubel, et al.
Leukemia|February 11, 2005
T(3;14)(p14.1;q32) involving IGH and FOXP1 is a novel recurrent chromosomal aberration in MALT lymphomaB Streubel, U Vinatzer, A Lamprecht, et al.
Gut|November 22, 2005
Successful antibiotic treatment of Helicobacter pylori negative gastric mucosa associated lymphoid tissue lymphomasM Raderer, B Streubel, S Wöhrer, et al.
Wiener Medizinische Wochenschrift (1946)|January 1, 1996
[In vitro transformation of amniotic cells to muscle cells--background and outlook]B Streubel, G Martucci-Ivessa, T Fleck, et al.
Leukemia|December 13, 2005
Novel t(5;9)(q33;q22) fuses ITK to SYK in unspecified peripheral T-cell lymphomaB Streubel, U Vinatzer, M Willheim, et al.
Gut|March 25, 2006
MALT lymphoma associated genetic aberrations occur at different frequencies in primary and secondary intestinal MALT lymphomasB Streubel, G Seitz, M Stolte, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|January 8, 2013
Prenatal microarray analysis as second-tier diagnostic test: single-center prospective studyM Schmid, S Stary, S Springer, et al.
Neuropediatrics|August 1, 1994
Coisogenic all-plus-one immunization: a model for identifying missing proteins in null-mutant conditions. Antibodies to dystrophin in mdx mouse after transplantation of muscle from normal coisogenic donorR E Bittner, B Streubel, S Shorny, et al.
American Journal of Medical Genetics|October 21, 1999
Somatic mosaicism of a greater than 1.7-Mb deletion of genomic DNA involving the entire NF1 gene as verified by FISH: further evidence for a contiguous gene syndrome in 17q11.2B Streubel, E Latta, H Kehrer-Sawatzki, et al.
Pageof 4