L C Strong|A G Knudson - JoVE Visualize

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American Journal of Human Genetics|August 1, 1992

Segregation analysis of cancer in families of childhood soft-tissue-sarcoma patientsE D Lustbader, W R Williams, M L Bondy, et al.

American Journal of Human Genetics|February 1, 1988

A genetic study of Gardner syndrome and congenital hypertrophy of the retinal pigment epitheliumL A Lyons, R A Lewis, L C Strong, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 22, 1994

Predisposition to renal carcinoma in the Eker rat is determined by germ-line mutation of the tuberous sclerosis 2 (TSC2) geneR S Yeung, G H Xiao, F Jin, et al.

Journal of Clinical Epidemiology|January 1, 1994

Accuracy of family history of cancer obtained through interviews with relatives of patients with childhood sarcomaM L Bondy, S S Strom, M W Colopy, et al.

Cancer Research|August 17, 2000

Renal failure in the Denys-Drash and Wilms' tumor-aniridia syndromesN E Breslow, J R Takashima, M L Ritchey, et al.

Cancer Research|January 1, 1997

Localization of a novel tumor suppressor locus on human chromosome 3q important in osteosarcoma tumorigenesisR P Kruzelock, E C Murphy, L C Strong, et al.

American Journal of Human Genetics|January 1, 1995

WT1 exon 1 deletion/insertion mutations in Wilms tumor patients, associated with di- and trinucleotide repeats and deletion hotspot consensus sequencesV Huff, N Jaffe, G F Saunders, et al.

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|August 1, 1987

Normal cytotoxic response of skin fibroblasts from patients with Li-Fraumeni familial cancer syndrome to DNA-damaging agents in vitroJ B Little, J Nove, W K Dahlberg, et al.

American Journal of Human Genetics|May 1, 1995

Hereditary multiple exostosis and chondrosarcoma: linkage to chromosome II and loss of heterozygosity for EXT-linked markers on chromosomes II and 8J T Hecht, D Hogue, L C Strong, et al.

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Showing results (81-90 of 128) with videos related to

Sort By:

Pageof 13

American Journal of Human Genetics|August 1, 1992

Segregation analysis of cancer in families of childhood soft-tissue-sarcoma patientsE D Lustbader, W R Williams, M L Bondy, et al.

American Journal of Human Genetics|February 1, 1988

A genetic study of Gardner syndrome and congenital hypertrophy of the retinal pigment epitheliumL A Lyons, R A Lewis, L C Strong, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 22, 1994

Predisposition to renal carcinoma in the Eker rat is determined by germ-line mutation of the tuberous sclerosis 2 (TSC2) geneR S Yeung, G H Xiao, F Jin, et al.

Journal of Clinical Epidemiology|January 1, 1994

Accuracy of family history of cancer obtained through interviews with relatives of patients with childhood sarcomaM L Bondy, S S Strom, M W Colopy, et al.

Cancer Research|August 17, 2000

Renal failure in the Denys-Drash and Wilms' tumor-aniridia syndromesN E Breslow, J R Takashima, M L Ritchey, et al.

Cancer Research|January 1, 1997

Localization of a novel tumor suppressor locus on human chromosome 3q important in osteosarcoma tumorigenesisR P Kruzelock, E C Murphy, L C Strong, et al.

American Journal of Human Genetics|January 1, 1995

WT1 exon 1 deletion/insertion mutations in Wilms tumor patients, associated with di- and trinucleotide repeats and deletion hotspot consensus sequencesV Huff, N Jaffe, G F Saunders, et al.

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|August 1, 1987

Normal cytotoxic response of skin fibroblasts from patients with Li-Fraumeni familial cancer syndrome to DNA-damaging agents in vitroJ B Little, J Nove, W K Dahlberg, et al.

American Journal of Human Genetics|May 1, 1995

Hereditary multiple exostosis and chondrosarcoma: linkage to chromosome II and loss of heterozygosity for EXT-linked markers on chromosomes II and 8J T Hecht, D Hogue, L C Strong, et al.

Pageof 13