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P J Morrison

Showing results (151-160 of 155) with videos related to

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Disease Markers|December 14, 1999
Guidelines for follow-up of women at high risk for inherited breast cancer: consensus statement from the Biomed 2 Demonstration Programme on Inherited Breast CancerP Møller, G Evans, N Haites, et al.
American Journal of Medical Genetics. Part A|June 5, 2003
Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington diseaseL Djoussé, B Knowlton, M Hayden, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|September 19, 2022
Analysis of rare disruptive germline mutations in 2135 enriched BRCA-negative breast cancers excludes additional high-impact susceptibility genesC Loveday, A Garrett, P Law, et al.
Human Molecular Genetics|May 23, 2003
Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiencyN A Alam, A J Rowan, N C Wortham, et al.
British Journal of Cancer|November 19, 2009
Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA)A Osorio, R L Milne, G Pita, et al.
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Showing results (151-160 of 155) with videos related to

Sort By:
Pageof 16
You have reached the last page of results.This site can display upto 155 results.
Disease Markers|December 14, 1999
Guidelines for follow-up of women at high risk for inherited breast cancer: consensus statement from the Biomed 2 Demonstration Programme on Inherited Breast CancerP Møller, G Evans, N Haites, et al.
American Journal of Medical Genetics. Part A|June 5, 2003
Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington diseaseL Djoussé, B Knowlton, M Hayden, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|September 19, 2022
Analysis of rare disruptive germline mutations in 2135 enriched BRCA-negative breast cancers excludes additional high-impact susceptibility genesC Loveday, A Garrett, P Law, et al.
Human Molecular Genetics|May 23, 2003
Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiencyN A Alam, A J Rowan, N C Wortham, et al.
British Journal of Cancer|November 19, 2009
Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA)A Osorio, R L Milne, G Pita, et al.
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