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Jeff Stevens

Showing results (21-30 of 28) with videos related to

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Journal of Neuro-Oncology|May 16, 2024
Detection of tumor-derived cell-free DNA in cerebrospinal fluid using a clinically validated targeted sequencing panel for pediatric brain tumorsRebecca Ronsley, Kristine A Karvonen, Bonnie Cole, et al.
International Journal of Cancer|March 14, 2023
A rare FGF5 candidate variant (rs112475347) for predisposition to nonsquamous, nonsmall-cell lung cancerLisa A Cannon-Albright, Craig C Teerlink, Jeff Stevens, et al.
Journal of Neurosurgery|November 26, 2022
A likely HOXC4 predisposition variant for Chiari malformationsDouglas L Brockmeyer, Samuel H Cheshier, Jeff Stevens, et al.
Birth Defects Research|March 24, 2018
Germline but not somatic de novo mutations are common in human congenital diaphragmatic herniaNori Matsunami, Hari Shanmugam, Lisa Baird, et al.
American Journal of Human Genetics|March 4, 2008
Neuropathy target esterase gene mutations cause motor neuron diseaseShirley Rainier, Melanie Bui, Erin Mark, et al.
Plos One|January 24, 2013
Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD populationNori Matsunami, Dexter Hadley, Charles H Hensel, et al.
Journal of the National Cancer Institute|April 17, 2018
A Nonsynonymous Variant in the GOLM1 Gene in Cutaneous Malignant MelanomaCraig C Teerlink, Chad Huff, Jeff Stevens, et al.
Molecular Autism|January 29, 2014
Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control populationNori Matsunami, Charles H Hensel, Lisa Baird, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Journal of Neuro-Oncology|May 16, 2024
Detection of tumor-derived cell-free DNA in cerebrospinal fluid using a clinically validated targeted sequencing panel for pediatric brain tumorsRebecca Ronsley, Kristine A Karvonen, Bonnie Cole, et al.
International Journal of Cancer|March 14, 2023
A rare FGF5 candidate variant (rs112475347) for predisposition to nonsquamous, nonsmall-cell lung cancerLisa A Cannon-Albright, Craig C Teerlink, Jeff Stevens, et al.
Journal of Neurosurgery|November 26, 2022
A likely HOXC4 predisposition variant for Chiari malformationsDouglas L Brockmeyer, Samuel H Cheshier, Jeff Stevens, et al.
Birth Defects Research|March 24, 2018
Germline but not somatic de novo mutations are common in human congenital diaphragmatic herniaNori Matsunami, Hari Shanmugam, Lisa Baird, et al.
American Journal of Human Genetics|March 4, 2008
Neuropathy target esterase gene mutations cause motor neuron diseaseShirley Rainier, Melanie Bui, Erin Mark, et al.
Plos One|January 24, 2013
Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD populationNori Matsunami, Dexter Hadley, Charles H Hensel, et al.
Journal of the National Cancer Institute|April 17, 2018
A Nonsynonymous Variant in the GOLM1 Gene in Cutaneous Malignant MelanomaCraig C Teerlink, Chad Huff, Jeff Stevens, et al.
Molecular Autism|January 29, 2014
Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control populationNori Matsunami, Charles H Hensel, Lisa Baird, et al.
Pageof 3