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F P Li

Showing results (201-210 of 211) with videos related to

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National Cancer Institute Monograph|December 1, 1985
A pilot vitamin intervention trial in Linxian, People's Republic of ChinaJ Y Li, G Y Li, S F Zheng, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1990
Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosisA G Menon, K M Anderson, V M Riccardi, et al.
JAMA|October 23, 1997
Cancer incidence after retinoblastoma. Radiation dose and sarcoma riskF L Wong, J D Boice, D H Abramson, et al.
Blood|June 15, 1996
Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 21q22.1-22.2C Y Ho, B Otterud, R D Legare, et al.
Cancer Research|October 28, 1999
Germ-line msh6 mutations in colorectal cancer familiesR D Kolodner, J D Tytell, J L Schmeits, et al.
Science (New York, N.Y.)|January 5, 2000
Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndromeD W Bell, J M Varley, T E Szydlo, et al.
Zhonghua Wei Chang Wai Ke Za Zhi = Chinese Journal of Gastrointestinal Surgery|July 15, 2024
[Effect of preoperative immune checkpoint inhibitors on reducing residual lymph node metastases in patients with gastric cancer: a retrospective study]X H Chen, H X Lin, Y H Chen, et al.
Cancer Research|November 24, 2001
Destabilization of CHK2 by a missense mutation associated with Li-Fraumeni SyndromeS B Lee, S H Kim, D W Bell, et al.
Clinical Genetics|July 31, 2007
Validation study of the LAMBDA model for predicting the BRCA1 or BRCA2 mutation carrier status of North American Ashkenazi Jewish womenC Apicella, J G Dowty, G S Dite, et al.
Nature Genetics|October 3, 1999
Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemiaW J Song, M G Sullivan, R D Legare, et al.
Pageof 22

Showing results (201-210 of 211) with videos related to

Sort By:
Pageof 22
National Cancer Institute Monograph|December 1, 1985
A pilot vitamin intervention trial in Linxian, People's Republic of ChinaJ Y Li, G Y Li, S F Zheng, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1990
Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosisA G Menon, K M Anderson, V M Riccardi, et al.
JAMA|October 23, 1997
Cancer incidence after retinoblastoma. Radiation dose and sarcoma riskF L Wong, J D Boice, D H Abramson, et al.
Blood|June 15, 1996
Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 21q22.1-22.2C Y Ho, B Otterud, R D Legare, et al.
Cancer Research|October 28, 1999
Germ-line msh6 mutations in colorectal cancer familiesR D Kolodner, J D Tytell, J L Schmeits, et al.
Science (New York, N.Y.)|January 5, 2000
Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndromeD W Bell, J M Varley, T E Szydlo, et al.
Zhonghua Wei Chang Wai Ke Za Zhi = Chinese Journal of Gastrointestinal Surgery|July 15, 2024
[Effect of preoperative immune checkpoint inhibitors on reducing residual lymph node metastases in patients with gastric cancer: a retrospective study]X H Chen, H X Lin, Y H Chen, et al.
Cancer Research|November 24, 2001
Destabilization of CHK2 by a missense mutation associated with Li-Fraumeni SyndromeS B Lee, S H Kim, D W Bell, et al.
Clinical Genetics|July 31, 2007
Validation study of the LAMBDA model for predicting the BRCA1 or BRCA2 mutation carrier status of North American Ashkenazi Jewish womenC Apicella, J G Dowty, G S Dite, et al.
Nature Genetics|October 3, 1999
Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemiaW J Song, M G Sullivan, R D Legare, et al.
Pageof 22