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J E Garber

Showing results (51-60 of 79) with videos related to

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Journal of the National Cancer Institute|December 21, 1988
Hepatoblastoma and familial adenomatous polyposisJ E Garber, F P Li, J E Kingston, et al.
Breast (Edinburgh, Scotland)|June 30, 2022
Moderate penetrance genes complicate genetic testing for breast cancer diagnosis: ATM, CHEK2, BARD1 and RAD51DR Graffeo, H Q Rana, F Conforti, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 1, 1995
Germline BRCA1 mutations and loss of the wild-type allele in tumors from families with early onset breast and ovarian cancerS D Merajver, T S Frank, J Xu, et al.
Genes, Chromosomes & Cancer|June 22, 2000
An Alu-mediated 7.1 kb deletion of BRCA1 exons 8 and 9 in breast and ovarian cancer families that results in alternative splicing of exon 10E M Rohlfs, N Puget, M L Graham, et al.
Archives of Internal Medicine|October 1, 1989
The impact of the prospective payment system on the treatment of hip fractures in the elderlyR M Palmer, R M Saywell, T W Zollinger, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|May 16, 2014
Phase I trial of olaparib in combination with cisplatin for the treatment of patients with advanced breast, ovarian and other solid tumorsJ Balmaña, N M Tung, S J Isakoff, et al.
Nature Genetics|December 1, 1994
Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancerL H Castilla, F J Couch, M R Erdos, et al.
American Journal of Human Genetics|January 1, 1995
An evaluation of genetic heterogeneity in 145 breast-ovarian cancer families. Breast Cancer Linkage ConsortiumS A Narod, D Ford, P Devilee, et al.
Oncogene|August 26, 1998
Germline mutations in PTEN are an infrequent cause of genetic predisposition to breast cancerM G FitzGerald, D J Marsh, D Wahrer, et al.
Annals of Internal Medicine|December 1, 1980
Waldenström's macroglobulinemia and autoimmune disease in a familyW A Blattner, J E Garber, D L Mann, et al.
Pageof 8

Showing results (51-60 of 79) with videos related to

Sort By:
Pageof 8
Journal of the National Cancer Institute|December 21, 1988
Hepatoblastoma and familial adenomatous polyposisJ E Garber, F P Li, J E Kingston, et al.
Breast (Edinburgh, Scotland)|June 30, 2022
Moderate penetrance genes complicate genetic testing for breast cancer diagnosis: ATM, CHEK2, BARD1 and RAD51DR Graffeo, H Q Rana, F Conforti, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 1, 1995
Germline BRCA1 mutations and loss of the wild-type allele in tumors from families with early onset breast and ovarian cancerS D Merajver, T S Frank, J Xu, et al.
Genes, Chromosomes & Cancer|June 22, 2000
An Alu-mediated 7.1 kb deletion of BRCA1 exons 8 and 9 in breast and ovarian cancer families that results in alternative splicing of exon 10E M Rohlfs, N Puget, M L Graham, et al.
Archives of Internal Medicine|October 1, 1989
The impact of the prospective payment system on the treatment of hip fractures in the elderlyR M Palmer, R M Saywell, T W Zollinger, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|May 16, 2014
Phase I trial of olaparib in combination with cisplatin for the treatment of patients with advanced breast, ovarian and other solid tumorsJ Balmaña, N M Tung, S J Isakoff, et al.
Nature Genetics|December 1, 1994
Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancerL H Castilla, F J Couch, M R Erdos, et al.
American Journal of Human Genetics|January 1, 1995
An evaluation of genetic heterogeneity in 145 breast-ovarian cancer families. Breast Cancer Linkage ConsortiumS A Narod, D Ford, P Devilee, et al.
Oncogene|August 26, 1998
Germline mutations in PTEN are an infrequent cause of genetic predisposition to breast cancerM G FitzGerald, D J Marsh, D Wahrer, et al.
Annals of Internal Medicine|December 1, 1980
Waldenström's macroglobulinemia and autoimmune disease in a familyW A Blattner, J E Garber, D L Mann, et al.
Pageof 8