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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 26, 2017
Do the data really support ordering fragile X testing as a first-tier test without clinical features?
Veronique Weinstein, Pranoot Tanpaiboon, Kimberly A Chapman, et al.
Journal of the National Comprehensive Cancer Network : JNCCN
|
December 11, 2023
Pilot Trial of Streamlined Genetic Education and Traceback Genetic Testing in Prostate Cancer Survivors
Marc D Schwartz, Beth N Peshkin, Claudine Isaacs, et al.
Cold Spring Harbor Molecular Case Studies
|
May 6, 2016
De novo POGZ mutations are associated with neurodevelopmental disorders and microcephaly
Yizhou Ye, Megan T Cho, Kyle Retterer, et al.
Translational Behavioral Medicine
|
November 13, 2018
Predictors of risk-reducing surgery intentions following genetic counseling for hereditary breast and ovarian cancer
Mary Kathleen Ladd, Beth N Peshkin, Leigha Senter, et al.
Human Genetics
|
September 30, 2016
De novo missense variants in PPP1CB are associated with intellectual disability and congenital heart disease
Lijiang Ma, Yavuz Bayram, Heather M McLaughlin, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 5) with videos related to
Sort By:
Page
of 1
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 26, 2017
Do the data really support ordering fragile X testing as a first-tier test without clinical features?
Veronique Weinstein, Pranoot Tanpaiboon, Kimberly A Chapman, et al.
Journal of the National Comprehensive Cancer Network : JNCCN
|
December 11, 2023
Pilot Trial of Streamlined Genetic Education and Traceback Genetic Testing in Prostate Cancer Survivors
Marc D Schwartz, Beth N Peshkin, Claudine Isaacs, et al.
Cold Spring Harbor Molecular Case Studies
|
May 6, 2016
De novo POGZ mutations are associated with neurodevelopmental disorders and microcephaly
Yizhou Ye, Megan T Cho, Kyle Retterer, et al.
Translational Behavioral Medicine
|
November 13, 2018
Predictors of risk-reducing surgery intentions following genetic counseling for hereditary breast and ovarian cancer
Mary Kathleen Ladd, Beth N Peshkin, Leigha Senter, et al.
Human Genetics
|
September 30, 2016
De novo missense variants in PPP1CB are associated with intellectual disability and congenital heart disease
Lijiang Ma, Yavuz Bayram, Heather M McLaughlin, et al.
Page
of 1