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American Journal of Human Genetics
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February 1, 2002
Individual-specific liability groups in genetic linkage, with applications to kindreds with Li-Fraumeni syndrome
Sanjay Shete, Christopher I Amos, Shih-Jen Hwang, et al.
Human Mutation
|
January 29, 2003
Missense mutations in the DNA-binding region and termination codon in PAX6
Lian-Yu Chao, Rajnikant Mishra, Louise C Strong, et al.
American Journal of Human Genetics
|
March 1, 2003
Germline p53 mutations in a cohort with childhood sarcoma: sex differences in cancer risk
Shih-Jen Hwang, Guillermina Lozano, Christopher I Amos, et al.
Science (New York, N.Y.)
|
May 28, 2016
CANCER. The cancer predisposition revolution
David Malkin, Judy E Garber, Louise C Strong, et al.
Mutation Research
|
December 1, 1992
Spontaneous and induced levels of chromosomal aberration and sister-chromatid exchange in neurofibromatosis: no evidence of chromosomal hypersensitivity
P Troilo, L C Strong, J B Little, et al.
Human Mutation
|
March 29, 2000
Mutation in the PAX6 gene in twenty patients with aniridia
L Y Chao, V Huff, L C Strong, et al.
Advances in Renal Replacement Therapy
|
July 1, 1995
Difficulty accepting lifestyle limitations after the abrupt onset of end-stage renal disease
M Wolfson, C Strong, K Hamel, et al.
Cancer Research
|
August 17, 2006
Joint effects of germ-line p53 mutation and sex on cancer risk in Li-Fraumeni syndrome
Chih-Chieh Wu, Sanjay Shete, Christopher I Amos, et al.
The New England Journal of Medicine
|
March 6, 1997
Germ-line mutations of the p53 tumor-suppressor gene in children and young adults with second malignant neoplasms
D Malkin, S H Friend, F P Li, et al.
Obstetrics and Gynecology
|
January 1, 1997
An approach to teaching ethical, legal, and psychosocial aspects of gynecologic oncology in a residency program
C Strong, B E Miller, G J Photopulos, et al.
Page
of 34
Search research articles
Search
Showing results (161-170 of 338) with videos related to
Sort By:
Page
of 34
American Journal of Human Genetics
|
February 1, 2002
Individual-specific liability groups in genetic linkage, with applications to kindreds with Li-Fraumeni syndrome
Sanjay Shete, Christopher I Amos, Shih-Jen Hwang, et al.
Human Mutation
|
January 29, 2003
Missense mutations in the DNA-binding region and termination codon in PAX6
Lian-Yu Chao, Rajnikant Mishra, Louise C Strong, et al.
American Journal of Human Genetics
|
March 1, 2003
Germline p53 mutations in a cohort with childhood sarcoma: sex differences in cancer risk
Shih-Jen Hwang, Guillermina Lozano, Christopher I Amos, et al.
Science (New York, N.Y.)
|
May 28, 2016
CANCER. The cancer predisposition revolution
David Malkin, Judy E Garber, Louise C Strong, et al.
Mutation Research
|
December 1, 1992
Spontaneous and induced levels of chromosomal aberration and sister-chromatid exchange in neurofibromatosis: no evidence of chromosomal hypersensitivity
P Troilo, L C Strong, J B Little, et al.
Human Mutation
|
March 29, 2000
Mutation in the PAX6 gene in twenty patients with aniridia
L Y Chao, V Huff, L C Strong, et al.
Advances in Renal Replacement Therapy
|
July 1, 1995
Difficulty accepting lifestyle limitations after the abrupt onset of end-stage renal disease
M Wolfson, C Strong, K Hamel, et al.
Cancer Research
|
August 17, 2006
Joint effects of germ-line p53 mutation and sex on cancer risk in Li-Fraumeni syndrome
Chih-Chieh Wu, Sanjay Shete, Christopher I Amos, et al.
The New England Journal of Medicine
|
March 6, 1997
Germ-line mutations of the p53 tumor-suppressor gene in children and young adults with second malignant neoplasms
D Malkin, S H Friend, F P Li, et al.
Obstetrics and Gynecology
|
January 1, 1997
An approach to teaching ethical, legal, and psychosocial aspects of gynecologic oncology in a residency program
C Strong, B E Miller, G J Photopulos, et al.
Page
of 34