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Journal of Genetic Counseling
|
April 26, 2015
"Not Tied Up Neatly with a Bow": Professionals' Challenging Cases in Informed Consent for Genomic Sequencing
Ashley N Tomlinson, Debra Skinner, Denise L Perry, et al.
American Journal of Medical Genetics. Part A
|
July 23, 2015
Experiences with obtaining informed consent for genomic sequencing
Barbara A Bernhardt, Myra I Roche, Denise L Perry, et al.
Journal of Animal Science
|
April 22, 2025
Relationship of tissue dimensions and stun placement on cadaver heads from 2-to-3-year-old male bison (Bison bison)
Allison L Matzek, Emma M Hamilton, Ashlynn A Kirk, et al.
Cold Spring Harbor Molecular Case Studies
|
November 5, 2021
Genome sequencing identifies three molecular diagnoses including a mosaic variant in the <i>COL2A1</i> gene in an individual with Pol III-related leukodystrophy and Feingold syndrome
Kayla J Muirhead, Amanda R Clause, Zinayida Schlachetzki, et al.
European Journal of Human Genetics : EJHG
|
April 2, 2024
A framework for the evaluation and reporting of incidental findings in clinical genomic testing
Carolyn M Brown, Laura M Amendola, Anjana Chandrasekhar, et al.
Journal of Empirical Research on Human Research Ethics : JERHRE
|
March 2, 2016
Participants and Study Decliners' Perspectives About the Risks of Participating in a Clinical Trial of Whole Genome Sequencing
Jill Oliver Robinson, Thomas M Carroll, Lindsay Z Feuerman, et al.
American Journal of Medical Genetics. Part A
|
November 6, 2023
Genome sequencing detects a balanced pericentric inversion with breakpoints that impact the DMD and upstream region of POU3F4 genes
Anjana Chandrasekhar, Henry J Mroczkowski, Nora Urraca, et al.
Cell Genomics
|
February 23, 2023
Reactive gene curation to support interpretation and reporting of a clinical genome test for rare disease: Experience from over 1,000 cases
Amanda R Clause, Julie P Taylor, Revathi Rajkumar, et al.
American Journal of Medical Genetics. Part A
|
June 7, 2022
PERCHING syndrome: Clinical presentation in the first African patient confirmed by clinical whole genome sequencing
Prince Makay, Gerrye Mubungu, Aimée Mupuala, et al.
American Journal of Medical Genetics. Part A
|
August 8, 2023
The smallest likely pathogenic duplication of a SOX9 enhancer identified to date in a family with 46,XX testicular differences of sex development
Samin A Sajan, Carolyn M Brown, Laura Davis-Keppen, et al.
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of 3
Search research articles
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Showing results (1-10 of 25) with videos related to
Sort By:
Page
of 3
Journal of Genetic Counseling
|
April 26, 2015
"Not Tied Up Neatly with a Bow": Professionals' Challenging Cases in Informed Consent for Genomic Sequencing
Ashley N Tomlinson, Debra Skinner, Denise L Perry, et al.
American Journal of Medical Genetics. Part A
|
July 23, 2015
Experiences with obtaining informed consent for genomic sequencing
Barbara A Bernhardt, Myra I Roche, Denise L Perry, et al.
Journal of Animal Science
|
April 22, 2025
Relationship of tissue dimensions and stun placement on cadaver heads from 2-to-3-year-old male bison (Bison bison)
Allison L Matzek, Emma M Hamilton, Ashlynn A Kirk, et al.
Cold Spring Harbor Molecular Case Studies
|
November 5, 2021
Genome sequencing identifies three molecular diagnoses including a mosaic variant in the <i>COL2A1</i> gene in an individual with Pol III-related leukodystrophy and Feingold syndrome
Kayla J Muirhead, Amanda R Clause, Zinayida Schlachetzki, et al.
European Journal of Human Genetics : EJHG
|
April 2, 2024
A framework for the evaluation and reporting of incidental findings in clinical genomic testing
Carolyn M Brown, Laura M Amendola, Anjana Chandrasekhar, et al.
Journal of Empirical Research on Human Research Ethics : JERHRE
|
March 2, 2016
Participants and Study Decliners' Perspectives About the Risks of Participating in a Clinical Trial of Whole Genome Sequencing
Jill Oliver Robinson, Thomas M Carroll, Lindsay Z Feuerman, et al.
American Journal of Medical Genetics. Part A
|
November 6, 2023
Genome sequencing detects a balanced pericentric inversion with breakpoints that impact the DMD and upstream region of POU3F4 genes
Anjana Chandrasekhar, Henry J Mroczkowski, Nora Urraca, et al.
Cell Genomics
|
February 23, 2023
Reactive gene curation to support interpretation and reporting of a clinical genome test for rare disease: Experience from over 1,000 cases
Amanda R Clause, Julie P Taylor, Revathi Rajkumar, et al.
American Journal of Medical Genetics. Part A
|
June 7, 2022
PERCHING syndrome: Clinical presentation in the first African patient confirmed by clinical whole genome sequencing
Prince Makay, Gerrye Mubungu, Aimée Mupuala, et al.
American Journal of Medical Genetics. Part A
|
August 8, 2023
The smallest likely pathogenic duplication of a SOX9 enhancer identified to date in a family with 46,XX testicular differences of sex development
Samin A Sajan, Carolyn M Brown, Laura Davis-Keppen, et al.
Page
of 3