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V Huff

Showing results (31-40 of 61) with videos related to

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The Journal of Urology|October 1, 1990
Familial renal cell carcinoma: hereditary or coincidental?A K Levinson, D E Johnson, L C Strong, et al.
Cancer Research|June 15, 1995
Sequential loss of heterozygosity at microsatellite motifs in preinvasive and invasive head and neck squamous carcinomaA K el-Naggar, K Hurr, J G Batsakis, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 1, 1996
Allelic loss and replication errors at microsatellite loci on chromosome 11p in head and neck squamous carcinoma: association with aggressive biological featuresA K El-Naggar, K Hurr, V Huff, et al.
Nature Genetics|February 1, 1993
Genetic mosaicism in normal tissues of Wilms' tumour patientsL Y Chao, V Huff, G Tomlinson, et al.
The American Journal of Pathology|June 1, 1996
Microsatellite instability in preinvasive and invasive head and neck squamous carcinomaA K El-Naggar, K Hurr, V Huff, et al.
Nature|November 24, 1988
Lack of linkage of familial Wilms' tumour to chromosomal band 11p13V Huff, D A Compton, L Y Chao, et al.
Pathogens and Global Health|December 20, 2021
Neurocysticercosis control for primary epilepsy prevention: a systematic reviewZhe Wang, Roxanna M Garcia, Hanalise V Huff, et al.
American Journal of Human Genetics|May 1, 1991
Evidence for WT1 as a Wilms tumor (WT) gene: intragenic germinal deletion in bilateral WTV Huff, H Miwa, D A Haber, et al.
Pediatric Nephrology (Berlin, Germany)|April 27, 2001
Pulmonary dysplasia, Denys-Drash syndrome and Wilms tumor 1 gene mutation in twinsV R Dharnidharka, E C Ruteshouser, S Rosen, et al.
Oncogene|December 22, 1999
Frequent loss of imprinting at the IGF2 and H19 genes in head and neck squamous carcinomaA K el-Naggar, S Lai, S A Tucker, et al.
Pageof 7

Showing results (31-40 of 61) with videos related to

Sort By:
Pageof 7
The Journal of Urology|October 1, 1990
Familial renal cell carcinoma: hereditary or coincidental?A K Levinson, D E Johnson, L C Strong, et al.
Cancer Research|June 15, 1995
Sequential loss of heterozygosity at microsatellite motifs in preinvasive and invasive head and neck squamous carcinomaA K el-Naggar, K Hurr, J G Batsakis, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 1, 1996
Allelic loss and replication errors at microsatellite loci on chromosome 11p in head and neck squamous carcinoma: association with aggressive biological featuresA K El-Naggar, K Hurr, V Huff, et al.
Nature Genetics|February 1, 1993
Genetic mosaicism in normal tissues of Wilms' tumour patientsL Y Chao, V Huff, G Tomlinson, et al.
The American Journal of Pathology|June 1, 1996
Microsatellite instability in preinvasive and invasive head and neck squamous carcinomaA K El-Naggar, K Hurr, V Huff, et al.
Nature|November 24, 1988
Lack of linkage of familial Wilms' tumour to chromosomal band 11p13V Huff, D A Compton, L Y Chao, et al.
Pathogens and Global Health|December 20, 2021
Neurocysticercosis control for primary epilepsy prevention: a systematic reviewZhe Wang, Roxanna M Garcia, Hanalise V Huff, et al.
American Journal of Human Genetics|May 1, 1991
Evidence for WT1 as a Wilms tumor (WT) gene: intragenic germinal deletion in bilateral WTV Huff, H Miwa, D A Haber, et al.
Pediatric Nephrology (Berlin, Germany)|April 27, 2001
Pulmonary dysplasia, Denys-Drash syndrome and Wilms tumor 1 gene mutation in twinsV R Dharnidharka, E C Ruteshouser, S Rosen, et al.
Oncogene|December 22, 1999
Frequent loss of imprinting at the IGF2 and H19 genes in head and neck squamous carcinomaA K el-Naggar, S Lai, S A Tucker, et al.
Pageof 7