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Journal of Genetic Counseling
|
September 28, 2021
Adapting skills from genetic counseling to wearables technology research during the COVID-19 pandemic: Poised for the pivot
Emily Higgs, Orit Dagan-Rosenfeld, Michael Snyder
Journal of Basic and Clinical Physiology and Pharmacology
|
November 16, 2005
Connexins in hearing loss: a comprehensive overview
Adi D Sabag, Orit Dagan, Karen B Avraham
American Journal of Medical Genetics
|
October 31, 2002
Genetic testing for hearing loss: different motivations for the same outcome
Orit Dagan, Hagit Hochner, Haya Levi, et al.
Journal of Genetic Counseling
|
March 6, 2019
Much ado about nothing: A qualitative study of the experiences of an average-risk population receiving results of exome sequencing
Shannon Rego, Orit Dagan-Rosenfeld, Stephanie A Bivona, et al.
Pediatric Research
|
March 19, 2004
The R245X mutation of PCDH15 in Ashkenazi Jewish children diagnosed with nonsyndromic hearing loss foreshadows retinitis pigmentosa
Zippora Brownstein, Tamar Ben-Yosef, Orit Dagan, et al.
Journal of Genetic Counseling
|
February 2, 2019
Developing a genomics rotation: Practical training around variant interpretation for genetic counseling students
Megan E Grove, Shana White, Dianna G Fisk, et al.
The Journal of Clinical Investigation
|
January 26, 2013
The LINC complex is essential for hearing
Henning F Horn, Zippora Brownstein, Danielle R Lenz, et al.
Cold Spring Harbor Molecular Case Studies
|
November 30, 2018
High-frequency actionable pathogenic exome variants in an average-risk cohort
Shannon Rego, Orit Dagan-Rosenfeld, Wenyu Zhou, et al.
American Journal of Human Genetics
|
July 7, 2010
Genomic duplication and overexpression of TJP2/ZO-2 leads to altered expression of apoptosis genes in progressive nonsyndromic hearing loss DFNA51
Tom Walsh, Sarah B Pierce, Danielle R Lenz, et al.
Biorxiv : the Preprint Server for Biology
|
May 27, 2024
Personalized transcriptome signatures in a cardiomyopathy stem cell biobank
Emma Monte, Takaaki Furihata, Guangwen Wang, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 19) with videos related to
Sort By:
Page
of 2
Journal of Genetic Counseling
|
September 28, 2021
Adapting skills from genetic counseling to wearables technology research during the COVID-19 pandemic: Poised for the pivot
Emily Higgs, Orit Dagan-Rosenfeld, Michael Snyder
Journal of Basic and Clinical Physiology and Pharmacology
|
November 16, 2005
Connexins in hearing loss: a comprehensive overview
Adi D Sabag, Orit Dagan, Karen B Avraham
American Journal of Medical Genetics
|
October 31, 2002
Genetic testing for hearing loss: different motivations for the same outcome
Orit Dagan, Hagit Hochner, Haya Levi, et al.
Journal of Genetic Counseling
|
March 6, 2019
Much ado about nothing: A qualitative study of the experiences of an average-risk population receiving results of exome sequencing
Shannon Rego, Orit Dagan-Rosenfeld, Stephanie A Bivona, et al.
Pediatric Research
|
March 19, 2004
The R245X mutation of PCDH15 in Ashkenazi Jewish children diagnosed with nonsyndromic hearing loss foreshadows retinitis pigmentosa
Zippora Brownstein, Tamar Ben-Yosef, Orit Dagan, et al.
Journal of Genetic Counseling
|
February 2, 2019
Developing a genomics rotation: Practical training around variant interpretation for genetic counseling students
Megan E Grove, Shana White, Dianna G Fisk, et al.
The Journal of Clinical Investigation
|
January 26, 2013
The LINC complex is essential for hearing
Henning F Horn, Zippora Brownstein, Danielle R Lenz, et al.
Cold Spring Harbor Molecular Case Studies
|
November 30, 2018
High-frequency actionable pathogenic exome variants in an average-risk cohort
Shannon Rego, Orit Dagan-Rosenfeld, Wenyu Zhou, et al.
American Journal of Human Genetics
|
July 7, 2010
Genomic duplication and overexpression of TJP2/ZO-2 leads to altered expression of apoptosis genes in progressive nonsyndromic hearing loss DFNA51
Tom Walsh, Sarah B Pierce, Danielle R Lenz, et al.
Biorxiv : the Preprint Server for Biology
|
May 27, 2024
Personalized transcriptome signatures in a cardiomyopathy stem cell biobank
Emma Monte, Takaaki Furihata, Guangwen Wang, et al.
Page
of 2