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David T Miller

Showing results (61-70 of 107) with videos related to

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Urologic Oncology|August 17, 2024
Factors influencing readmission patterns following radical cystectomy: An analysis of social determinants and discharge outcomesValentina Grajales, Jonathan Y Lin, Danielle Sharbaugh, et al.
BMC Genomics|December 18, 2014
Chromosome microarray testing for patients with congenital heart defects reveals novel disease causing loci and high diagnostic yieldJuan Geng, Jonathan Picker, Zhaojing Zheng, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 10, 2017
Loss of Twist1 in the Mesenchymal Compartment Promotes Increased Fibrosis in Experimental Lung Injury by Enhanced Expression of CXCL12Jiangning Tan, John R Tedrow, Mehdi Nouraie, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 22, 2008
SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing lossPu Dai, Qi Li, Deliang Huang, et al.
Urology|September 4, 2023
A Multipronged Intervention to Reduce Readmissions and Readmission Intensity After Radical CystectomyZeynep G Gul, Shan Wu, Michael Raver, et al.
American Journal of Medical Genetics. Part A|June 11, 2016
BRAT1 mutations present with a spectrum of clinical severitySiddharth Srivastava, Heather E Olson, Julie S Cohen, et al.
Clinical Chemistry|September 29, 2007
Development of a focused oligonucleotide-array comparative genomic hybridization chip for clinical diagnosis of genomic imbalanceYiping Shen, Mira Irons, David T Miller, et al.
American Journal of Human Genetics|May 4, 2020
Insufficient Evidence for "Autism-Specific" GenesScott M Myers, Thomas D Challman, Raphael Bernier, et al.
The Journal of Molecular Diagnostics : JMD|January 23, 2010
Genome-wide oligonucleotide array comparative genomic hybridization for etiological diagnosis of mental retardation: a multicenter experience of 1499 clinical casesBixia Xiang, Hongbo Zhu, Yiping Shen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 31, 2024
Consideration of disease penetrance in the selection of secondary findings gene-disease pairs: A policy statement of the American College of Medical Genetics and Genomics (ACMG)Adam S Gordon, Kristy Lee, Noura S Abul-Husn, et al.
Pageof 11

Showing results (61-70 of 107) with videos related to

Sort By:
Pageof 11
Urologic Oncology|August 17, 2024
Factors influencing readmission patterns following radical cystectomy: An analysis of social determinants and discharge outcomesValentina Grajales, Jonathan Y Lin, Danielle Sharbaugh, et al.
BMC Genomics|December 18, 2014
Chromosome microarray testing for patients with congenital heart defects reveals novel disease causing loci and high diagnostic yieldJuan Geng, Jonathan Picker, Zhaojing Zheng, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 10, 2017
Loss of Twist1 in the Mesenchymal Compartment Promotes Increased Fibrosis in Experimental Lung Injury by Enhanced Expression of CXCL12Jiangning Tan, John R Tedrow, Mehdi Nouraie, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 22, 2008
SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing lossPu Dai, Qi Li, Deliang Huang, et al.
Urology|September 4, 2023
A Multipronged Intervention to Reduce Readmissions and Readmission Intensity After Radical CystectomyZeynep G Gul, Shan Wu, Michael Raver, et al.
American Journal of Medical Genetics. Part A|June 11, 2016
BRAT1 mutations present with a spectrum of clinical severitySiddharth Srivastava, Heather E Olson, Julie S Cohen, et al.
Clinical Chemistry|September 29, 2007
Development of a focused oligonucleotide-array comparative genomic hybridization chip for clinical diagnosis of genomic imbalanceYiping Shen, Mira Irons, David T Miller, et al.
American Journal of Human Genetics|May 4, 2020
Insufficient Evidence for "Autism-Specific" GenesScott M Myers, Thomas D Challman, Raphael Bernier, et al.
The Journal of Molecular Diagnostics : JMD|January 23, 2010
Genome-wide oligonucleotide array comparative genomic hybridization for etiological diagnosis of mental retardation: a multicenter experience of 1499 clinical casesBixia Xiang, Hongbo Zhu, Yiping Shen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 31, 2024
Consideration of disease penetrance in the selection of secondary findings gene-disease pairs: A policy statement of the American College of Medical Genetics and Genomics (ACMG)Adam S Gordon, Kristy Lee, Noura S Abul-Husn, et al.
Pageof 11