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Oncogene
|
August 26, 1998
Telomerase activity during spontaneous immortalization of Li-Fraumeni syndrome skin fibroblasts
L S Gollahon, E Kraus, T A Wu, et al.
Internal Medicine Journal
|
December 6, 2003
Novel p53 germline mutation in a patient with Li-Fraumeni syndrome
S S Wong, G Lozano, C L Gaff, et al.
Human Genetics
|
August 14, 1998
Exclusion of a p53 germline mutation in a classic Li-Fraumeni syndrome family
S C Evans, B Mims, K M McMasters, et al.
Oncogene
|
February 1, 1991
Tumorigenic transformation of spontaneously immortalized fibroblasts from patients with a familial cancer syndrome
F Z Bischoff, L C Strong, S O Yim, et al.
Cancer Research
|
April 16, 1998
Linkage of familial Wilms' tumor predisposition to chromosome 19 and a two-locus model for the etiology of familial tumors
J M McDonald, E C Douglass, R Fisher, et al.
American Journal of Human Genetics
|
January 1, 1997
Hereditary multiple exostoses (EXT): mutational studies of familial EXT1 cases and EXT-associated malignancies
J T Hecht, D Hogue, Y Wang, et al.
American Journal of Human Genetics
|
May 1, 1987
Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors
W T Schroeder, L Y Chao, D D Dao, et al.
Cancer Research
|
December 15, 1990
Spontaneous abnormalities in normal fibroblasts from patients with Li-Fraumeni cancer syndrome: aneuploidy and immortalization
F Z Bischoff, S O Yim, S Pathak, et al.
Cancer
|
May 15, 1993
Long-term survival. Clinical care, research, and education
A T Meadows, B Black, M E Nesbit, et al.
Genomics
|
February 1, 1990
Definition of the limits of the Wilms tumor locus on human chromosome 11p13
D A Compton, M M Weil, L Bonetta, et al.
Page
of 15
Search research articles
Search
Showing results (121-130 of 145) with videos related to
Sort By:
Page
of 15
Oncogene
|
August 26, 1998
Telomerase activity during spontaneous immortalization of Li-Fraumeni syndrome skin fibroblasts
L S Gollahon, E Kraus, T A Wu, et al.
Internal Medicine Journal
|
December 6, 2003
Novel p53 germline mutation in a patient with Li-Fraumeni syndrome
S S Wong, G Lozano, C L Gaff, et al.
Human Genetics
|
August 14, 1998
Exclusion of a p53 germline mutation in a classic Li-Fraumeni syndrome family
S C Evans, B Mims, K M McMasters, et al.
Oncogene
|
February 1, 1991
Tumorigenic transformation of spontaneously immortalized fibroblasts from patients with a familial cancer syndrome
F Z Bischoff, L C Strong, S O Yim, et al.
Cancer Research
|
April 16, 1998
Linkage of familial Wilms' tumor predisposition to chromosome 19 and a two-locus model for the etiology of familial tumors
J M McDonald, E C Douglass, R Fisher, et al.
American Journal of Human Genetics
|
January 1, 1997
Hereditary multiple exostoses (EXT): mutational studies of familial EXT1 cases and EXT-associated malignancies
J T Hecht, D Hogue, Y Wang, et al.
American Journal of Human Genetics
|
May 1, 1987
Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors
W T Schroeder, L Y Chao, D D Dao, et al.
Cancer Research
|
December 15, 1990
Spontaneous abnormalities in normal fibroblasts from patients with Li-Fraumeni cancer syndrome: aneuploidy and immortalization
F Z Bischoff, S O Yim, S Pathak, et al.
Cancer
|
May 15, 1993
Long-term survival. Clinical care, research, and education
A T Meadows, B Black, M E Nesbit, et al.
Genomics
|
February 1, 1990
Definition of the limits of the Wilms tumor locus on human chromosome 11p13
D A Compton, M M Weil, L Bonetta, et al.
Page
of 15