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American Journal of Human Genetics
|
February 1, 1988
A genetic study of Gardner syndrome and congenital hypertrophy of the retinal pigment epithelium
L A Lyons, R A Lewis, L C Strong, et al.
Journal of Clinical Epidemiology
|
January 1, 1994
Accuracy of family history of cancer obtained through interviews with relatives of patients with childhood sarcoma
M 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 syndromes
N 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 tumorigenesis
R 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 sequences
V Huff, N Jaffe, G F Saunders, 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 vitro
J 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 8
J T Hecht, D Hogue, L C Strong, 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.
Journal of the National Cancer Institute
|
August 1, 1984
Cancer mortality in relatives of retinoblastoma patients
L C Strong, J Herson, C Haas, et al.
Nature Genetics
|
February 1, 1993
Genetic mosaicism in normal tissues of Wilms' tumour patients
L Y Chao, V Huff, G Tomlinson, et al.
Page
of 15
Search research articles
Search
Showing results (101-110 of 145) with videos related to
Sort By:
Page
of 15
American Journal of Human Genetics
|
February 1, 1988
A genetic study of Gardner syndrome and congenital hypertrophy of the retinal pigment epithelium
L A Lyons, R A Lewis, L C Strong, et al.
Journal of Clinical Epidemiology
|
January 1, 1994
Accuracy of family history of cancer obtained through interviews with relatives of patients with childhood sarcoma
M 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 syndromes
N 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 tumorigenesis
R 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 sequences
V Huff, N Jaffe, G F Saunders, 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 vitro
J 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 8
J T Hecht, D Hogue, L C Strong, 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.
Journal of the National Cancer Institute
|
August 1, 1984
Cancer mortality in relatives of retinoblastoma patients
L C Strong, J Herson, C Haas, et al.
Nature Genetics
|
February 1, 1993
Genetic mosaicism in normal tissues of Wilms' tumour patients
L Y Chao, V Huff, G Tomlinson, et al.
Page
of 15