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B B Biesecker

Showing results (31-40 of 37) with videos related to

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Clinical Genetics|June 15, 2012
Effects of informed consent for individual genome sequencing on relevant knowledgeK A Kaphingst, F M Facio, M-R Cheng, et al.
Clinical Genetics|February 21, 2017
Defining personal utility in genomics: A Delphi studyJ N Kohler, E Turbitt, K L Lewis, et al.
JAMA|May 14, 1997
Genetic testing for susceptibility to adult-onset cancer. The process and content of informed consentG Geller, J R Botkin, M J Green, et al.
Clinical Genetics|December 8, 2016
PUGS: A novel scale to assess perceptions of uncertainties in genome sequencingB B Biesecker, S W Woolford, W M P Klein, et al.
Clinical Genetics|April 15, 2018
Correction to: PUGS: A novel scale to assess perceptions of uncertainties in genome sequencingB B Biesecker, S W Woolford, W M P Klein, et al.
Nature Genetics|February 1, 1994
A disease locus for hereditary haemorrhagic telangiectasia maps to chromosome 9q33-34M T McDonald, K A Papenberg, S Ghosh, et al.
Clinical Genetics|February 1, 2018
Disclosure of cardiac variants of uncertain significance results in an exome cohortT A Lawal, K L Lewis, J J Johnston, et al.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Clinical Genetics|June 15, 2012
Effects of informed consent for individual genome sequencing on relevant knowledgeK A Kaphingst, F M Facio, M-R Cheng, et al.
Clinical Genetics|February 21, 2017
Defining personal utility in genomics: A Delphi studyJ N Kohler, E Turbitt, K L Lewis, et al.
JAMA|May 14, 1997
Genetic testing for susceptibility to adult-onset cancer. The process and content of informed consentG Geller, J R Botkin, M J Green, et al.
Clinical Genetics|December 8, 2016
PUGS: A novel scale to assess perceptions of uncertainties in genome sequencingB B Biesecker, S W Woolford, W M P Klein, et al.
Clinical Genetics|April 15, 2018
Correction to: PUGS: A novel scale to assess perceptions of uncertainties in genome sequencingB B Biesecker, S W Woolford, W M P Klein, et al.
Nature Genetics|February 1, 1994
A disease locus for hereditary haemorrhagic telangiectasia maps to chromosome 9q33-34M T McDonald, K A Papenberg, S Ghosh, et al.
Clinical Genetics|February 1, 2018
Disclosure of cardiac variants of uncertain significance results in an exome cohortT A Lawal, K L Lewis, J J Johnston, et al.
Pageof 4