Search research articles
Contact Us
Filters
Showing results (71-80 of 82) with videos related to
Page
of 9
Sort By:
Urology Practice
|
October 10, 2025
Persistent Sex Disparities in Bladder Cancer Diagnosis: An Analysis of National Trends From 2012 to 2021
Edward Z Zhang, Jack C Millot, Adithya Balasubramanian, et al.
JAMA Network Open
|
October 21, 2024
Use of Preferred Source of Contraception Among Users of the Pill, Patch, and Ring in the US
Anu Manchikanti Gomez, Ariana H Bennett, Alex Schulte, et al.
Nature Communications
|
July 1, 2025
An mRNA vaccine encoding five conserved Group A Streptococcus antigens
Nichaela Harbison-Price, Ismail Sebina, Rhiannon A Bolton, et al.
American Journal of Human Genetics
|
July 31, 2020
Variants in SCAF4 Cause a Neurodevelopmental Disorder and Are Associated with Impaired mRNA Processing
Anna Fliedner, Philipp Kirchner, Antje Wiesener, et al.
HGG Advances
|
April 8, 2025
Multiple molecular diagnoses identified through genome sequencing in individuals with suspected rare disease
Alka Malhotra, Erin Thorpe, Alison J Coffey, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 16, 2023
Clinical, neuroradiological, and molecular characterization of mitochondrial threonyl-tRNA-synthetase (TARS2)-related disorder
Andrea Accogli, Sheng-Jia Lin, Mariasavina Severino, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 18, 2020
GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder
Christine Shieh, Natasha Jones, Brigitte Vanle, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 13, 2020
Correction: GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder
Christine Shieh, Natasha Jones, Brigitte Vanle, et al.
American Journal of Human Genetics
|
June 6, 2024
The impact of clinical genome sequencing in a global population with suspected rare genetic disease
Erin Thorpe, Taylor Williams, Chad Shaw, et al.
American Journal of Human Genetics
|
November 4, 2017
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies
Fadi F Hamdan, Candace T Myers, Patrick Cossette, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 82) with videos related to
Sort By:
Page
of 9
Urology Practice
|
October 10, 2025
Persistent Sex Disparities in Bladder Cancer Diagnosis: An Analysis of National Trends From 2012 to 2021
Edward Z Zhang, Jack C Millot, Adithya Balasubramanian, et al.
JAMA Network Open
|
October 21, 2024
Use of Preferred Source of Contraception Among Users of the Pill, Patch, and Ring in the US
Anu Manchikanti Gomez, Ariana H Bennett, Alex Schulte, et al.
Nature Communications
|
July 1, 2025
An mRNA vaccine encoding five conserved Group A Streptococcus antigens
Nichaela Harbison-Price, Ismail Sebina, Rhiannon A Bolton, et al.
American Journal of Human Genetics
|
July 31, 2020
Variants in SCAF4 Cause a Neurodevelopmental Disorder and Are Associated with Impaired mRNA Processing
Anna Fliedner, Philipp Kirchner, Antje Wiesener, et al.
HGG Advances
|
April 8, 2025
Multiple molecular diagnoses identified through genome sequencing in individuals with suspected rare disease
Alka Malhotra, Erin Thorpe, Alison J Coffey, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 16, 2023
Clinical, neuroradiological, and molecular characterization of mitochondrial threonyl-tRNA-synthetase (TARS2)-related disorder
Andrea Accogli, Sheng-Jia Lin, Mariasavina Severino, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 18, 2020
GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder
Christine Shieh, Natasha Jones, Brigitte Vanle, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 13, 2020
Correction: GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder
Christine Shieh, Natasha Jones, Brigitte Vanle, et al.
American Journal of Human Genetics
|
June 6, 2024
The impact of clinical genome sequencing in a global population with suspected rare genetic disease
Erin Thorpe, Taylor Williams, Chad Shaw, et al.
American Journal of Human Genetics
|
November 4, 2017
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies
Fadi F Hamdan, Candace T Myers, Patrick Cossette, et al.
Page
of 9