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Science (New York, N.Y.)
|
August 10, 2002
Recent segmental duplications in the human genome
Jeffrey A Bailey, Zhiping Gu, Royden A Clark, et al.
Trials
|
March 26, 2021
Hematologists' barriers and enablers to screening and recruiting patients to a chimeric antigen receptor (CAR) T cell therapy trial: a theory-informed interview study
Gisell Castillo, Manoj Lalu, Sarah Asad, et al.
American Journal of Medical Genetics. Part A
|
May 3, 2023
Uniparental disomy of multiple chromosomes in two cases with a complex phenotype
Katarzyna Polonis, Jaime L Lopes, Huong Cabral, et al.
American Journal of Medical Genetics. Part A
|
April 24, 2013
Clinical comparison of overlapping deletions of 19p13.3
Hiba Risheg, Romela Pasion, Stephanie Sacharow, et al.
Genome Research
|
June 21, 2005
Punctuated duplication seeding events during the evolution of human chromosome 2p11
Julie E Horvath, Cassandra L Gulden, Rhea U Vallente, et al.
American Journal of Human Genetics
|
July 11, 2006
Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome
Devin P Locke, Andrew J Sharp, Steven A McCarroll, et al.
BMJ Open
|
March 20, 2021
Navigating choice in the face of uncertainty: using a theory informed qualitative approach to identifying potential patient barriers and enablers to participating in an early phase chimeric antigen receptor T (CAR-T) cell therapy trial
Gisell Castillo, Manoj M Lalu, Sarah Asad, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 20, 2018
Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
Darrel Waggoner, Karen E Wain, Adrian M Dubuc, et al.
Research Involvement and Engagement
|
October 19, 2020
Partnering with patients to get better outcomes with chimeric antigen receptor T-cell therapy: towards engagement of patients in early phase trials
Madison Foster, Dean A Fergusson, Terry Hawrysh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 12, 2009
Variability in interpreting and reporting copy number changes detected by array-based technology in clinical laboratories
Karen D Tsuchiya, Lisa G Shaffer, Swaroop Aradhya, et al.
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Search research articles
Search
Showing results (51-60 of 73) with videos related to
Sort By:
Page
of 8
Science (New York, N.Y.)
|
August 10, 2002
Recent segmental duplications in the human genome
Jeffrey A Bailey, Zhiping Gu, Royden A Clark, et al.
Trials
|
March 26, 2021
Hematologists' barriers and enablers to screening and recruiting patients to a chimeric antigen receptor (CAR) T cell therapy trial: a theory-informed interview study
Gisell Castillo, Manoj Lalu, Sarah Asad, et al.
American Journal of Medical Genetics. Part A
|
May 3, 2023
Uniparental disomy of multiple chromosomes in two cases with a complex phenotype
Katarzyna Polonis, Jaime L Lopes, Huong Cabral, et al.
American Journal of Medical Genetics. Part A
|
April 24, 2013
Clinical comparison of overlapping deletions of 19p13.3
Hiba Risheg, Romela Pasion, Stephanie Sacharow, et al.
Genome Research
|
June 21, 2005
Punctuated duplication seeding events during the evolution of human chromosome 2p11
Julie E Horvath, Cassandra L Gulden, Rhea U Vallente, et al.
American Journal of Human Genetics
|
July 11, 2006
Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome
Devin P Locke, Andrew J Sharp, Steven A McCarroll, et al.
BMJ Open
|
March 20, 2021
Navigating choice in the face of uncertainty: using a theory informed qualitative approach to identifying potential patient barriers and enablers to participating in an early phase chimeric antigen receptor T (CAR-T) cell therapy trial
Gisell Castillo, Manoj M Lalu, Sarah Asad, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 20, 2018
Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
Darrel Waggoner, Karen E Wain, Adrian M Dubuc, et al.
Research Involvement and Engagement
|
October 19, 2020
Partnering with patients to get better outcomes with chimeric antigen receptor T-cell therapy: towards engagement of patients in early phase trials
Madison Foster, Dean A Fergusson, Terry Hawrysh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 12, 2009
Variability in interpreting and reporting copy number changes detected by array-based technology in clinical laboratories
Karen D Tsuchiya, Lisa G Shaffer, Swaroop Aradhya, et al.
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of 8