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P Dane Witmer

Showing results (11-20 of 23) with videos related to

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Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|January 6, 2018
Pancreatic Juice Mutation Concentrations Can Help Predict the Grade of Dysplasia in Patients Undergoing Pancreatic SurveillanceMasaya Suenaga, Jun Yu, Koji Shindo, et al.
Current Protocols in Human Genetics|January 12, 2017
Generating Exome Enriched Sequencing Libraries from Formalin-Fixed, Paraffin-Embedded Tissue DNA for Next-Generation SequencingBeth A Marosy, Brian D Craig, Kurt N Hetrick, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 24, 2013
Inactivation of the microRNA-183/96/182 cluster results in syndromic retinal degenerationStephen Lumayag, Caroline E Haldin, Nicola J Corbett, et al.
American Journal of Medical Genetics. Part A|November 15, 2014
Truncating mutations in the last exon of NOTCH3 cause lateral meningocele syndromeKaren W Gripp, Katherine M Robbins, Nara L Sobreira, et al.
Human Mutation|July 15, 2021
Variants of human CLDN9 cause mild to profound hearing lossMemoona Ramzan, Christophe Philippe, Inna A Belyantseva, et al.
Journal of the American College of Cardiology|August 4, 2018
Clinical Validity of Genes for Heritable Thoracic Aortic Aneurysm and DissectionMarjolijn Renard, Catherine Francis, Rajarshi Ghosh, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 3, 2017
Deleterious Germline Mutations in Patients With Apparently Sporadic Pancreatic AdenocarcinomaKoji Shindo, Jun Yu, Masaya Suenaga, et al.
Journal of Clinical Immunology|July 9, 2020
Deficiency of Adenosine Deaminase 2 (DADA2): Hidden Variants, Reduced Penetrance, and Unusual InheritanceOskar Schnappauf, Qing Zhou, Natalia Sampaio Moura, et al.
Scientific Reports|May 5, 2026
Genetic studies identify known and novel variants for recessively inherited moderate to severe hearing loss in consanguineous families from PakistanMemoona Ramzan, Hafiza Idrees, Hina Khan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 19, 2019
Insights into genetics, human biology and disease gleaned from family based genomic studiesJennifer E Posey, Anne H O'Donnell-Luria, Jessica X Chong, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

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Pageof 3
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|January 6, 2018
Pancreatic Juice Mutation Concentrations Can Help Predict the Grade of Dysplasia in Patients Undergoing Pancreatic SurveillanceMasaya Suenaga, Jun Yu, Koji Shindo, et al.
Current Protocols in Human Genetics|January 12, 2017
Generating Exome Enriched Sequencing Libraries from Formalin-Fixed, Paraffin-Embedded Tissue DNA for Next-Generation SequencingBeth A Marosy, Brian D Craig, Kurt N Hetrick, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 24, 2013
Inactivation of the microRNA-183/96/182 cluster results in syndromic retinal degenerationStephen Lumayag, Caroline E Haldin, Nicola J Corbett, et al.
American Journal of Medical Genetics. Part A|November 15, 2014
Truncating mutations in the last exon of NOTCH3 cause lateral meningocele syndromeKaren W Gripp, Katherine M Robbins, Nara L Sobreira, et al.
Human Mutation|July 15, 2021
Variants of human CLDN9 cause mild to profound hearing lossMemoona Ramzan, Christophe Philippe, Inna A Belyantseva, et al.
Journal of the American College of Cardiology|August 4, 2018
Clinical Validity of Genes for Heritable Thoracic Aortic Aneurysm and DissectionMarjolijn Renard, Catherine Francis, Rajarshi Ghosh, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 3, 2017
Deleterious Germline Mutations in Patients With Apparently Sporadic Pancreatic AdenocarcinomaKoji Shindo, Jun Yu, Masaya Suenaga, et al.
Journal of Clinical Immunology|July 9, 2020
Deficiency of Adenosine Deaminase 2 (DADA2): Hidden Variants, Reduced Penetrance, and Unusual InheritanceOskar Schnappauf, Qing Zhou, Natalia Sampaio Moura, et al.
Scientific Reports|May 5, 2026
Genetic studies identify known and novel variants for recessively inherited moderate to severe hearing loss in consanguineous families from PakistanMemoona Ramzan, Hafiza Idrees, Hina Khan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 19, 2019
Insights into genetics, human biology and disease gleaned from family based genomic studiesJennifer E Posey, Anne H O'Donnell-Luria, Jessica X Chong, et al.
Pageof 3