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Catherine E Cottrell

Showing results (11-20 of 72) with videos related to

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Experimental and Molecular Pathology|January 18, 2017
Spectrum of mutations in leiomyosarcomas identified by clinical targeted next-generation sequencingPaul J Lee, Naomi S Yoo, Ian S Hagemann, et al.
European Journal of Medical Genetics|August 16, 2019
Genotype-phenotype correlation: Inheritance and variant-type infer pathogenicity in IQSEC2 geneElizabeth S Barrie, Catherine E Cottrell, Julie Gastier-Foster, et al.
Cold Spring Harbor Molecular Case Studies|August 25, 2017
<i>FGFR2</i> amplification in colorectal adenocarcinomaJamal H Carter, Catherine E Cottrell, Samantha N McNulty, et al.
The Journal of Molecular Diagnostics : JMD|January 3, 2017
Targeted Next-Generation Sequencing in Molecular Subtyping of Lower-Grade Diffuse Gliomas: Application of the World Health Organization's 2016 Revised Criteria for Central Nervous System TumorsJamal H Carter, Samantha N McNulty, Patrick J Cimino, et al.
American Journal of Medical Genetics. Part A|February 14, 2009
Atypical X-chromosome inactivation in an X;1 translocation patient demonstrating Xq28 functional disomyCatherine E Cottrell, Annemarie Sommer, Gail D Wenger, et al.
Journal of the National Comprehensive Cancer Network : JNCCN|October 19, 2021
Targeted Therapy in a Young Adult With a Novel Epithelioid Tumor Driven by a PRRC2B-ALK FusionAjay Gupta, Huifei Liu, Kathleen M Schieffer, et al.
Pediatric Dermatology|December 29, 2021
KRIT1-positive hyperkeratotic cutaneous capillary venous malformationBayan Matarneh, Catherine E Cottrell, Samantha Choi, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|July 29, 2017
Routine use of clinical exome-based next-generation sequencing for evaluation of patients with thrombotic microangiopathiesJoseph P Gaut, Sanjay Jain, John D Pfeifer, et al.
Cold Spring Harbor Molecular Case Studies|February 27, 2021
Clinical response to dabrafenib plus trametinib in a pediatric ganglioglioma with <i>BRAF</i> p.T599dup mutationKatherine E Miller, Kathleen M Schieffer, Olivia Grischow, et al.
The Journal of Molecular Diagnostics : JMD|December 12, 2022
Assessments of Somatic Variant Classification Using the Association for Molecular Pathology/American Society of Clinical Oncology/College of American Pathologists Guidelines: A Report from the Association for Molecular PathologyMarilyn M Li, Catherine E Cottrell, Mrudula Pullambhatla, et al.
Pageof 8

Showing results (11-20 of 72) with videos related to

Sort By:
Pageof 8
Experimental and Molecular Pathology|January 18, 2017
Spectrum of mutations in leiomyosarcomas identified by clinical targeted next-generation sequencingPaul J Lee, Naomi S Yoo, Ian S Hagemann, et al.
European Journal of Medical Genetics|August 16, 2019
Genotype-phenotype correlation: Inheritance and variant-type infer pathogenicity in IQSEC2 geneElizabeth S Barrie, Catherine E Cottrell, Julie Gastier-Foster, et al.
Cold Spring Harbor Molecular Case Studies|August 25, 2017
<i>FGFR2</i> amplification in colorectal adenocarcinomaJamal H Carter, Catherine E Cottrell, Samantha N McNulty, et al.
The Journal of Molecular Diagnostics : JMD|January 3, 2017
Targeted Next-Generation Sequencing in Molecular Subtyping of Lower-Grade Diffuse Gliomas: Application of the World Health Organization's 2016 Revised Criteria for Central Nervous System TumorsJamal H Carter, Samantha N McNulty, Patrick J Cimino, et al.
American Journal of Medical Genetics. Part A|February 14, 2009
Atypical X-chromosome inactivation in an X;1 translocation patient demonstrating Xq28 functional disomyCatherine E Cottrell, Annemarie Sommer, Gail D Wenger, et al.
Journal of the National Comprehensive Cancer Network : JNCCN|October 19, 2021
Targeted Therapy in a Young Adult With a Novel Epithelioid Tumor Driven by a PRRC2B-ALK FusionAjay Gupta, Huifei Liu, Kathleen M Schieffer, et al.
Pediatric Dermatology|December 29, 2021
KRIT1-positive hyperkeratotic cutaneous capillary venous malformationBayan Matarneh, Catherine E Cottrell, Samantha Choi, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|July 29, 2017
Routine use of clinical exome-based next-generation sequencing for evaluation of patients with thrombotic microangiopathiesJoseph P Gaut, Sanjay Jain, John D Pfeifer, et al.
Cold Spring Harbor Molecular Case Studies|February 27, 2021
Clinical response to dabrafenib plus trametinib in a pediatric ganglioglioma with <i>BRAF</i> p.T599dup mutationKatherine E Miller, Kathleen M Schieffer, Olivia Grischow, et al.
The Journal of Molecular Diagnostics : JMD|December 12, 2022
Assessments of Somatic Variant Classification Using the Association for Molecular Pathology/American Society of Clinical Oncology/College of American Pathologists Guidelines: A Report from the Association for Molecular PathologyMarilyn M Li, Catherine E Cottrell, Mrudula Pullambhatla, et al.
Pageof 8