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Marilu Nelson

Showing results (11-20 of 36) with videos related to

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Human Pathology|June 13, 2015
Papillary tumor of the pineal region with synchronous suprasellar focus and novel cytogenetic featuresBret C Mobley, Manoj Kumar, Warren G Sanger, et al.
Cancer Genetics and Cytogenetics|October 3, 2006
A (9;11)(q34;q13) translocation in a hibernomaKiran K Turaga, Edibaldo Silva-Lopez, Warren G Sanger, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|November 16, 2010
Renal cell carcinoma with novel VCL-ALK fusion: new representative of ALK-associated tumor spectrumLarisa V Debelenko, Susana C Raimondi, Najat Daw, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|February 24, 2012
Translocation t(12;17)(q24.1;q21) as the sole anomaly in a nasal chondromesenchymal hamartoma arising in a patient with pleuropulmonary blastomaRadwa El Behery, Jiri Bedrnicek, Audrey Lazenby, et al.
The Journal of Molecular Diagnostics : JMD|July 24, 2003
Inconspicuous insertion 22;12 in myxoid/round cell liposarcoma accompanied by the secondary structural abnormality der(16)t(1;16)Nathan C Birch, Cristina R Antonescu, Marilu Nelson, et al.
Cancer Genetics and Cytogenetics|February 12, 2008
Lack of a common or characteristic cytogenetic anomaly in solitary fibrous tumorAlireza Torabi, Subodh M Lele, Dominick DiMaio, et al.
American Journal of Medical Genetics. Part A|August 17, 2005
Cryptic duplication and deletion of 9q34.3 --> qter in a family with a t(9;22)(q34.3;p11.2)Travis M Sanger, Ann Haskins Olney, Dianna Zaleski, et al.
Archives of Pathology & Laboratory Medicine|December 8, 2009
Detection of chromosomal aberrations in renal tumors: a comparative study of conventional cytogenetics and virtual karyotyping with single-nucleotide polymorphism microarraysFederico A Monzon, Karla Alvarez, Zoran Gatalica, et al.
Experimental and Molecular Pathology|September 9, 2006
Chronic idiopathic myelofibrosis (CIMF) resulting from a unique 3;9 translocation disrupting the janus kinase 2 (JAK2) geneHon Fong L Mark, Edgar A Sotomayor, Marilu Nelson, et al.
Genes, Chromosomes & Cancer|July 8, 2010
C11orf95-MKL2 is the resulting fusion oncogene of t(11;16)(q13;p13) in chondroid lipomaDali Huang, Janos Sumegi, Paola Dal Cin, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
Human Pathology|June 13, 2015
Papillary tumor of the pineal region with synchronous suprasellar focus and novel cytogenetic featuresBret C Mobley, Manoj Kumar, Warren G Sanger, et al.
Cancer Genetics and Cytogenetics|October 3, 2006
A (9;11)(q34;q13) translocation in a hibernomaKiran K Turaga, Edibaldo Silva-Lopez, Warren G Sanger, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|November 16, 2010
Renal cell carcinoma with novel VCL-ALK fusion: new representative of ALK-associated tumor spectrumLarisa V Debelenko, Susana C Raimondi, Najat Daw, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|February 24, 2012
Translocation t(12;17)(q24.1;q21) as the sole anomaly in a nasal chondromesenchymal hamartoma arising in a patient with pleuropulmonary blastomaRadwa El Behery, Jiri Bedrnicek, Audrey Lazenby, et al.
The Journal of Molecular Diagnostics : JMD|July 24, 2003
Inconspicuous insertion 22;12 in myxoid/round cell liposarcoma accompanied by the secondary structural abnormality der(16)t(1;16)Nathan C Birch, Cristina R Antonescu, Marilu Nelson, et al.
Cancer Genetics and Cytogenetics|February 12, 2008
Lack of a common or characteristic cytogenetic anomaly in solitary fibrous tumorAlireza Torabi, Subodh M Lele, Dominick DiMaio, et al.
American Journal of Medical Genetics. Part A|August 17, 2005
Cryptic duplication and deletion of 9q34.3 --> qter in a family with a t(9;22)(q34.3;p11.2)Travis M Sanger, Ann Haskins Olney, Dianna Zaleski, et al.
Archives of Pathology & Laboratory Medicine|December 8, 2009
Detection of chromosomal aberrations in renal tumors: a comparative study of conventional cytogenetics and virtual karyotyping with single-nucleotide polymorphism microarraysFederico A Monzon, Karla Alvarez, Zoran Gatalica, et al.
Experimental and Molecular Pathology|September 9, 2006
Chronic idiopathic myelofibrosis (CIMF) resulting from a unique 3;9 translocation disrupting the janus kinase 2 (JAK2) geneHon Fong L Mark, Edgar A Sotomayor, Marilu Nelson, et al.
Genes, Chromosomes & Cancer|July 8, 2010
C11orf95-MKL2 is the resulting fusion oncogene of t(11;16)(q13;p13) in chondroid lipomaDali Huang, Janos Sumegi, Paola Dal Cin, et al.
Pageof 4