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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 19, 2022
Response to Ramos et al
Eleanor G Seaby, Diana Baralle, Heidi L Rehm, et al.
The Annals of Otology, Rhinology, and Laryngology
|
September 2, 2005
Audiologic features of Norrie disease
Chris Halpin, Grace Owen, Gustavo A Gutiérrez-Espeleta, et al.
The Laryngoscope
|
February 8, 2011
Temporal bone abnormalities in children with GJB2 mutations
Margaret A Kenna, Heidi L Rehm, Anna Frangulov, et al.
Human Mutation
|
October 13, 2018
Updated recommendation for the benign stand-alone ACMG/AMP criterion
Rajarshi Ghosh, Steven M Harrison, Heidi L Rehm, et al.
The Journal of Molecular Diagnostics : JMD
|
January 1, 2013
Inherited cardiomyopathies: molecular genetics and clinical genetic testing in the postgenomic era
Polakit Teekakirikul, Melissa A Kelly, Heidi L Rehm, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 8, 2024
Correspondence on "Comparison of literature mining tools for variant classification: Through the lens of 50 RYR1 variants" by Wermers et al
Chih-Hsuan Wei, Lon Phan, Timothy Hefferon, et al.
Frontiers in Genetics
|
December 6, 2021
TMPRSS3 Gene Variants With Implications for Auditory Treatment and Counseling
In Seok Moon, Andrew R Grant, Varun Sagi, et al.
American Journal of Medical Genetics. Part A
|
July 13, 2012
Norrie disease: extraocular clinical manifestations in 56 patients
Sharon E Smith, Thomas E Mullen, Dionne Graham, et al.
Health Affairs (Project Hope)
|
May 8, 2018
Lack Of Diversity In Genomic Databases Is A Barrier To Translating Precision Medicine Research Into Practice
Latrice G Landry, Nadya Ali, David R Williams, et al.
Current Protocols in Human Genetics
|
April 11, 2009
An overview of custom array sequencing
Prachi Kothiyal, Stephanie Cox, Jonathan Ebert, et al.
Page
of 35
Search research articles
Search
Showing results (41-50 of 342) with videos related to
Sort By:
Page
of 35
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 19, 2022
Response to Ramos et al
Eleanor G Seaby, Diana Baralle, Heidi L Rehm, et al.
The Annals of Otology, Rhinology, and Laryngology
|
September 2, 2005
Audiologic features of Norrie disease
Chris Halpin, Grace Owen, Gustavo A Gutiérrez-Espeleta, et al.
The Laryngoscope
|
February 8, 2011
Temporal bone abnormalities in children with GJB2 mutations
Margaret A Kenna, Heidi L Rehm, Anna Frangulov, et al.
Human Mutation
|
October 13, 2018
Updated recommendation for the benign stand-alone ACMG/AMP criterion
Rajarshi Ghosh, Steven M Harrison, Heidi L Rehm, et al.
The Journal of Molecular Diagnostics : JMD
|
January 1, 2013
Inherited cardiomyopathies: molecular genetics and clinical genetic testing in the postgenomic era
Polakit Teekakirikul, Melissa A Kelly, Heidi L Rehm, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 8, 2024
Correspondence on "Comparison of literature mining tools for variant classification: Through the lens of 50 RYR1 variants" by Wermers et al
Chih-Hsuan Wei, Lon Phan, Timothy Hefferon, et al.
Frontiers in Genetics
|
December 6, 2021
TMPRSS3 Gene Variants With Implications for Auditory Treatment and Counseling
In Seok Moon, Andrew R Grant, Varun Sagi, et al.
American Journal of Medical Genetics. Part A
|
July 13, 2012
Norrie disease: extraocular clinical manifestations in 56 patients
Sharon E Smith, Thomas E Mullen, Dionne Graham, et al.
Health Affairs (Project Hope)
|
May 8, 2018
Lack Of Diversity In Genomic Databases Is A Barrier To Translating Precision Medicine Research Into Practice
Latrice G Landry, Nadya Ali, David R Williams, et al.
Current Protocols in Human Genetics
|
April 11, 2009
An overview of custom array sequencing
Prachi Kothiyal, Stephanie Cox, Jonathan Ebert, et al.
Page
of 35