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R Bartram

Showing results (261-270 of 393) with videos related to

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British Journal of Haematology|May 1, 1995
The fusion of TEL and ABL in human acute lymphoblastic leukaemia is a rare eventJ W Janssen, S A Ridge, P Papadopoulos, et al.
American Journal of Medical Genetics. Part A|May 11, 2017
Diagnosis of CoPAN by whole exome sequencing: Waking up a sleeping tiger's eyeChristina Evers, Angelika Seitz, Birgit Assmann, et al.
Leukemia Research|December 5, 2008
Functional analysis of a novel DNA polymorphism of a tandem repeated sequence in the asparagine synthetase gene in acute lymphoblastic leukemia cellsTadayuki Akagi, Dong Yin, Norihiko Kawamata, et al.
Blood|August 27, 2005
CD10- pre-B acute lymphoblastic leukemia (ALL) is a distinct high-risk subgroup of adult ALL associated with a high frequency of MLL aberrations: results of the German Multicenter Trials for Adult ALL (GMALL)Beate Gleissner, Nicola Goekbuget, Harald Rieder, et al.
Genome Medicine|August 1, 2015
So rare we need to hunt for them: reframing the ethical debate on incidental findingsSebastian Schuol, Christoph Schickhardt, Stefan Wiemann, et al.
Oncogene|October 10, 2003
Allelotype analysis in relapsed childhood acute lymphoblastic leukemiaSeisho Takeuchi, Taku Seriu, Jacques J M van Dongen, et al.
Leukemia Research|July 26, 2005
Aberrant methylation in promoter-associated CpG islands of multiple genes in acute lymphoblastic leukemiaYang Yang, Seisho Takeuchi, Wolf K Hofmann, et al.
Annals of Hematology|January 24, 2009
Quantification of free total plasma DNA and minimal residual disease detection in the plasma of children with acute lymphoblastic leukemiaArne Kristian Schwarz, Martin Stanulla, Gunnar Cario, et al.
Frontiers in Physiology|March 13, 2019
The Frog <i>Xenopus</i> as a Model to Study Joubert Syndrome: The Case of a Human Patient With Compound Heterozygous Variants in <i>PIBF1</i>Tim Ott, Lilian Kaufmann, Martin Granzow, et al.
Leukemia|September 1, 1994
t(5;14)(q33-34;q11), a new recurring cytogenetic abnormality in childhood acute leukemiaJ A Whitlock, S C Raimondi, J Harbott, et al.
Pageof 40

Showing results (261-270 of 393) with videos related to

Sort By:
Pageof 40
British Journal of Haematology|May 1, 1995
The fusion of TEL and ABL in human acute lymphoblastic leukaemia is a rare eventJ W Janssen, S A Ridge, P Papadopoulos, et al.
American Journal of Medical Genetics. Part A|May 11, 2017
Diagnosis of CoPAN by whole exome sequencing: Waking up a sleeping tiger's eyeChristina Evers, Angelika Seitz, Birgit Assmann, et al.
Leukemia Research|December 5, 2008
Functional analysis of a novel DNA polymorphism of a tandem repeated sequence in the asparagine synthetase gene in acute lymphoblastic leukemia cellsTadayuki Akagi, Dong Yin, Norihiko Kawamata, et al.
Blood|August 27, 2005
CD10- pre-B acute lymphoblastic leukemia (ALL) is a distinct high-risk subgroup of adult ALL associated with a high frequency of MLL aberrations: results of the German Multicenter Trials for Adult ALL (GMALL)Beate Gleissner, Nicola Goekbuget, Harald Rieder, et al.
Genome Medicine|August 1, 2015
So rare we need to hunt for them: reframing the ethical debate on incidental findingsSebastian Schuol, Christoph Schickhardt, Stefan Wiemann, et al.
Oncogene|October 10, 2003
Allelotype analysis in relapsed childhood acute lymphoblastic leukemiaSeisho Takeuchi, Taku Seriu, Jacques J M van Dongen, et al.
Leukemia Research|July 26, 2005
Aberrant methylation in promoter-associated CpG islands of multiple genes in acute lymphoblastic leukemiaYang Yang, Seisho Takeuchi, Wolf K Hofmann, et al.
Annals of Hematology|January 24, 2009
Quantification of free total plasma DNA and minimal residual disease detection in the plasma of children with acute lymphoblastic leukemiaArne Kristian Schwarz, Martin Stanulla, Gunnar Cario, et al.
Frontiers in Physiology|March 13, 2019
The Frog <i>Xenopus</i> as a Model to Study Joubert Syndrome: The Case of a Human Patient With Compound Heterozygous Variants in <i>PIBF1</i>Tim Ott, Lilian Kaufmann, Martin Granzow, et al.
Leukemia|September 1, 1994
t(5;14)(q33-34;q11), a new recurring cytogenetic abnormality in childhood acute leukemiaJ A Whitlock, S C Raimondi, J Harbott, et al.
Pageof 40