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Tom Walsh

Showing results (161-170 of 193) with videos related to

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The Journal of Molecular Diagnostics : JMD|November 6, 2013
Validation and implementation of targeted capture and sequencing for the detection of actionable mutation, copy number variation, and gene rearrangement in clinical cancer specimensColin C Pritchard, Stephen J Salipante, Karen Koehler, et al.
Genome Biology|September 16, 2011
Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in Middle Eastern familiesZippora Brownstein, Lilach M Friedman, Hashem Shahin, et al.
The Journal of Molecular Diagnostics : JMD|June 5, 2012
ColoSeq provides comprehensive lynch and polyposis syndrome mutational analysis using massively parallel sequencingColin C Pritchard, Christina Smith, Stephen J Salipante, et al.
Journal of Medical Genetics|July 29, 2021
Diagnostic yield of chromosomal microarray and trio whole exome sequencing in cryptogenic cerebral palsyMichal Yechieli, Suleyman Gulsuner, Hilla Ben-Pazi, et al.
Blood|June 1, 2017
Bone marrow failure unresponsive to bone marrow transplant is caused by mutations in <i>thrombopoietin</i>Aaron Seo, Miri Ben-Harosh, Mehtap Sirin, et al.
JAMA Oncology|January 1, 2016
Inherited Mutations in Women With Ovarian CarcinomaBarbara M Norquist, Maria I Harrell, Mark F Brady, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 2, 2017
Mutations in Homologous Recombination Genes and Outcomes in Ovarian Carcinoma Patients in GOG 218: An NRG Oncology/Gynecologic Oncology Group StudyBarbara M Norquist, Mark F Brady, Maria I Harrell, et al.
The Journal of Clinical Endocrinology and Metabolism|March 17, 2015
Homozygous loss-of-function mutations in SOHLH1 in patients with nonsyndromic hypergonadotropic hypogonadismYavuz Bayram, Suleyman Gulsuner, Tulay Guran, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 25, 2013
Mutation of the ATP-gated P2X(2) receptor leads to progressive hearing loss and increased susceptibility to noiseDenise Yan, Yan Zhu, Tom Walsh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 5, 2016
Improving performance of multigene panels for genomic analysis of cancer predispositionBrian H Shirts, Silvia Casadei, Angela L Jacobson, et al.
Pageof 20

Showing results (161-170 of 193) with videos related to

Sort By:
Pageof 20
The Journal of Molecular Diagnostics : JMD|November 6, 2013
Validation and implementation of targeted capture and sequencing for the detection of actionable mutation, copy number variation, and gene rearrangement in clinical cancer specimensColin C Pritchard, Stephen J Salipante, Karen Koehler, et al.
Genome Biology|September 16, 2011
Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in Middle Eastern familiesZippora Brownstein, Lilach M Friedman, Hashem Shahin, et al.
The Journal of Molecular Diagnostics : JMD|June 5, 2012
ColoSeq provides comprehensive lynch and polyposis syndrome mutational analysis using massively parallel sequencingColin C Pritchard, Christina Smith, Stephen J Salipante, et al.
Journal of Medical Genetics|July 29, 2021
Diagnostic yield of chromosomal microarray and trio whole exome sequencing in cryptogenic cerebral palsyMichal Yechieli, Suleyman Gulsuner, Hilla Ben-Pazi, et al.
Blood|June 1, 2017
Bone marrow failure unresponsive to bone marrow transplant is caused by mutations in <i>thrombopoietin</i>Aaron Seo, Miri Ben-Harosh, Mehtap Sirin, et al.
JAMA Oncology|January 1, 2016
Inherited Mutations in Women With Ovarian CarcinomaBarbara M Norquist, Maria I Harrell, Mark F Brady, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 2, 2017
Mutations in Homologous Recombination Genes and Outcomes in Ovarian Carcinoma Patients in GOG 218: An NRG Oncology/Gynecologic Oncology Group StudyBarbara M Norquist, Mark F Brady, Maria I Harrell, et al.
The Journal of Clinical Endocrinology and Metabolism|March 17, 2015
Homozygous loss-of-function mutations in SOHLH1 in patients with nonsyndromic hypergonadotropic hypogonadismYavuz Bayram, Suleyman Gulsuner, Tulay Guran, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 25, 2013
Mutation of the ATP-gated P2X(2) receptor leads to progressive hearing loss and increased susceptibility to noiseDenise Yan, Yan Zhu, Tom Walsh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 5, 2016
Improving performance of multigene panels for genomic analysis of cancer predispositionBrian H Shirts, Silvia Casadei, Angela L Jacobson, et al.
Pageof 20