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A R Brothman

Showing results (51-60 of 78) with videos related to

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Cancer Genetics and Cytogenetics|June 1, 1997
Myelodysplastic syndrome presenting with clonal rearrangement isolated to chromosomal region 1qM J Mogul, K Brady, A R Brothman, et al.
International Journal of Cancer|September 1, 1994
Tumorigenicity of SV40 T antigen immortalized human prostate epithelial cells: association with decreased epidermal growth factor receptor (EGFR) expressionV L Bae, C K Jackson-Cook, A R Brothman, et al.
Nature Genetics|March 1, 1995
Mutation of the MXI1 gene in prostate cancerL R Eagle, X Yin, A R Brothman, et al.
Neurology|December 1, 1992
Trisomy 17p associated with Charcot-Marie-Tooth neuropathy type 1A phenotype: evidence for gene dosage as a mechanism in CMT1AP F Chance, T D Bird, N Matsunami, et al.
Journal of Pediatric Hematology/Oncology|April 17, 1998
Spindle cell sarcoma of the kidney with ganglionic elements (malignant ectomesenchymoma) associated with chromosomal abnormalities and a review of the literatureR E Goldsby, C S Bruggers, A R Brothman, et al.
Cancer Genetics and Cytogenetics|February 1, 1989
Cytogenetic analysis of four primary prostatic culturesA R Brothman, L J Lesho, K D Somers, et al.
American Journal of Medical Genetics. Part A|March 11, 2005
Karyotype/phenotype correlations in duplication 4q: evidence for a critical region within 4q27-28 for preaxial defectsA Battaglia, Z Chen, A R Brothman, et al.
Cytogenetics and Cell Genetics|January 1, 1996
The detection of contiguous gene deletions at the neurofibromatosis 1 locus with fluorescence in situ hybridizationK A Leppig, D Viskochil, S Neil, et al.
The Journal of Urology|February 1, 1996
Evidence for a tumor suppressor gene distal to BRCA1 in prostate cancerB J Williams, E Jones, X L Zhu, et al.
Journal of Medical Genetics|March 19, 2009
U-type exchange is the most frequent mechanism for inverted duplication with terminal deletion rearrangementsL R Rowe, J-Y Lee, L Rector, et al.
Pageof 8

Showing results (51-60 of 78) with videos related to

Sort By:
Pageof 8
Cancer Genetics and Cytogenetics|June 1, 1997
Myelodysplastic syndrome presenting with clonal rearrangement isolated to chromosomal region 1qM J Mogul, K Brady, A R Brothman, et al.
International Journal of Cancer|September 1, 1994
Tumorigenicity of SV40 T antigen immortalized human prostate epithelial cells: association with decreased epidermal growth factor receptor (EGFR) expressionV L Bae, C K Jackson-Cook, A R Brothman, et al.
Nature Genetics|March 1, 1995
Mutation of the MXI1 gene in prostate cancerL R Eagle, X Yin, A R Brothman, et al.
Neurology|December 1, 1992
Trisomy 17p associated with Charcot-Marie-Tooth neuropathy type 1A phenotype: evidence for gene dosage as a mechanism in CMT1AP F Chance, T D Bird, N Matsunami, et al.
Journal of Pediatric Hematology/Oncology|April 17, 1998
Spindle cell sarcoma of the kidney with ganglionic elements (malignant ectomesenchymoma) associated with chromosomal abnormalities and a review of the literatureR E Goldsby, C S Bruggers, A R Brothman, et al.
Cancer Genetics and Cytogenetics|February 1, 1989
Cytogenetic analysis of four primary prostatic culturesA R Brothman, L J Lesho, K D Somers, et al.
American Journal of Medical Genetics. Part A|March 11, 2005
Karyotype/phenotype correlations in duplication 4q: evidence for a critical region within 4q27-28 for preaxial defectsA Battaglia, Z Chen, A R Brothman, et al.
Cytogenetics and Cell Genetics|January 1, 1996
The detection of contiguous gene deletions at the neurofibromatosis 1 locus with fluorescence in situ hybridizationK A Leppig, D Viskochil, S Neil, et al.
The Journal of Urology|February 1, 1996
Evidence for a tumor suppressor gene distal to BRCA1 in prostate cancerB J Williams, E Jones, X L Zhu, et al.
Journal of Medical Genetics|March 19, 2009
U-type exchange is the most frequent mechanism for inverted duplication with terminal deletion rearrangementsL R Rowe, J-Y Lee, L Rector, et al.
Pageof 8