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Clinics in Laboratory Medicine
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May 23, 2020
Enhancing Diagnosis Through RNA Sequencing
David R Murdock
Annual Review of Medicine
|
January 27, 2022
What Has the Undiagnosed Diseases Network Taught Us About the Clinical Applications of Genomic Testing?
David R Murdock, Jill A Rosenfeld, Brendan Lee
Journal of Biomechanics
|
February 28, 2006
Studies of plasma membrane mechanics and plasma membrane-cytoskeleton interactions using optical tweezers and fluorescence imaging
Sergey A Ermilov, David R Murdock, Feng Qian, et al.
Journal of Neurophysiology
|
June 17, 2005
Effects of salicylate on plasma membrane mechanics
Sergey A Ermilov, David R Murdock, Dania El-Daye, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 22, 2017
Whole-Exome Sequencing for Diagnosis of Turner Syndrome: Toward Next-Generation Sequencing and Newborn Screening
David R Murdock, Frank X Donovan, Settara C Chandrasekharappa, et al.
Biophysical Journal
|
October 4, 2005
Effects of chlorpromazine on mechanical properties of the outer hair cell plasma membrane
David R Murdock, Sergey A Ermilov, Alexander A Spector, et al.
American Journal of Medical Genetics. Part A
|
January 31, 2023
Further delineation of the CWC27-associated spliceosomeopathy: Case report and review of the literature
Shaden H Yassin, Riley Henderson, Jerica Lenberg, et al.
Genetics in Medicine Open
|
June 27, 2025
Early diagnosis of vascular Ehlers-Danlos syndrome through AI-powered facial analysis: Results from the Montalcino Aortic Consortium
David R Murdock, Adarsh Suresh, Ernesto Calderon Martinez, et al.
Cold Spring Harbor Molecular Case Studies
|
January 10, 2019
Xia-Gibbs syndrome in adulthood: a case report with insight into the natural history of the condition
David R Murdock, Yunyun Jiang, Michael Wangler, et al.
American Journal of Medical Genetics. Part A
|
August 12, 2011
Whole-exome sequencing identifies compound heterozygous mutations in WDR62 in siblings with recurrent polymicrogyria
David R Murdock, Gary D Clark, Matthew N Bainbridge, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 48) with videos related to
Sort By:
Page
of 5
Clinics in Laboratory Medicine
|
May 23, 2020
Enhancing Diagnosis Through RNA Sequencing
David R Murdock
Annual Review of Medicine
|
January 27, 2022
What Has the Undiagnosed Diseases Network Taught Us About the Clinical Applications of Genomic Testing?
David R Murdock, Jill A Rosenfeld, Brendan Lee
Journal of Biomechanics
|
February 28, 2006
Studies of plasma membrane mechanics and plasma membrane-cytoskeleton interactions using optical tweezers and fluorescence imaging
Sergey A Ermilov, David R Murdock, Feng Qian, et al.
Journal of Neurophysiology
|
June 17, 2005
Effects of salicylate on plasma membrane mechanics
Sergey A Ermilov, David R Murdock, Dania El-Daye, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 22, 2017
Whole-Exome Sequencing for Diagnosis of Turner Syndrome: Toward Next-Generation Sequencing and Newborn Screening
David R Murdock, Frank X Donovan, Settara C Chandrasekharappa, et al.
Biophysical Journal
|
October 4, 2005
Effects of chlorpromazine on mechanical properties of the outer hair cell plasma membrane
David R Murdock, Sergey A Ermilov, Alexander A Spector, et al.
American Journal of Medical Genetics. Part A
|
January 31, 2023
Further delineation of the CWC27-associated spliceosomeopathy: Case report and review of the literature
Shaden H Yassin, Riley Henderson, Jerica Lenberg, et al.
Genetics in Medicine Open
|
June 27, 2025
Early diagnosis of vascular Ehlers-Danlos syndrome through AI-powered facial analysis: Results from the Montalcino Aortic Consortium
David R Murdock, Adarsh Suresh, Ernesto Calderon Martinez, et al.
Cold Spring Harbor Molecular Case Studies
|
January 10, 2019
Xia-Gibbs syndrome in adulthood: a case report with insight into the natural history of the condition
David R Murdock, Yunyun Jiang, Michael Wangler, et al.
American Journal of Medical Genetics. Part A
|
August 12, 2011
Whole-exome sequencing identifies compound heterozygous mutations in WDR62 in siblings with recurrent polymicrogyria
David R Murdock, Gary D Clark, Matthew N Bainbridge, et al.
Page
of 5