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Blood
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October 13, 2016
Alternative genetic mechanisms of BRAF activation in Langerhans cell histiocytosis
Rikhia Chakraborty, Thomas M Burke, Oliver A Hampton, et al.
Hematological Oncology
|
February 21, 2017
The use of BRAF V600E mutation-specific immunohistochemistry in pediatric Langerhans cell histiocytosis
Leomar Y Ballester, Miguel D Cantu, Karen P H Lim, et al.
Genome Medicine
|
November 6, 2016
Somatic cancer variant curation and harmonization through consensus minimum variant level data
Deborah I Ritter, Sameek Roychowdhury, Angshumoy Roy, et al.
Cancer Genetics
|
January 13, 2022
Distinct somatic DICER1 hotspot mutations in three metachronous ovarian Sertoli-Leydig cell tumors in a patient with DICER1 syndrome
Annie Garcia, Lauren Desrosiers, Sarah Scollon, et al.
Pediatric Blood & Cancer
|
June 17, 2022
Clinical and molecular features of pediatric cancer patients with Lynch syndrome
Sarah Scollon, Mohammad K Eldomery, Jacquelyn Reuther, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
November 1, 2014
BCOR-CCNB3 fusions are frequent in undifferentiated sarcomas of male children
Tricia L Peters, Vijetha Kumar, Sumanth Polikepahad, et al.
Human Mutation
|
October 13, 2018
Adapting crowdsourced clinical cancer curation in CIViC to the ClinGen minimum variant level data community-driven standards
Arpad M Danos, Deborah I Ritter, Alex H Wagner, et al.
Pediatric Blood & Cancer
|
October 3, 2020
Integrated DNA and RNA sequencing reveals targetable alterations in metastatic pediatric papillary thyroid carcinoma
Samara L Potter, Jacquelyn Reuther, Raghu Chandramohan, et al.
JCO Precision Oncology
|
October 15, 2021
Durable Response to Larotrectinib in a Child With Histologic Diagnosis of Recurrent Disseminated Ependymoma Discovered to Harbor an <i>NTRK2</i> Fusion: The Impact of Integrated Genomic Profiling
Ross Mangum, Jacquelyn Reuther, Kelsey C Bertrand, et al.
Cancer Genetics
|
February 22, 2025
Anaplastic meningioma in a 6-year-old with somatic YAP1::MAML2 fusion and multiple endocrine neoplasia type 4 (MEN4) syndrome
Lauren R Desrosiers-Battu, John H Lee, Izabela Tarasiewicz, et al.
Page
of 10
Search research articles
Search
Showing results (71-80 of 92) with videos related to
Sort By:
Page
of 10
Blood
|
October 13, 2016
Alternative genetic mechanisms of BRAF activation in Langerhans cell histiocytosis
Rikhia Chakraborty, Thomas M Burke, Oliver A Hampton, et al.
Hematological Oncology
|
February 21, 2017
The use of BRAF V600E mutation-specific immunohistochemistry in pediatric Langerhans cell histiocytosis
Leomar Y Ballester, Miguel D Cantu, Karen P H Lim, et al.
Genome Medicine
|
November 6, 2016
Somatic cancer variant curation and harmonization through consensus minimum variant level data
Deborah I Ritter, Sameek Roychowdhury, Angshumoy Roy, et al.
Cancer Genetics
|
January 13, 2022
Distinct somatic DICER1 hotspot mutations in three metachronous ovarian Sertoli-Leydig cell tumors in a patient with DICER1 syndrome
Annie Garcia, Lauren Desrosiers, Sarah Scollon, et al.
Pediatric Blood & Cancer
|
June 17, 2022
Clinical and molecular features of pediatric cancer patients with Lynch syndrome
Sarah Scollon, Mohammad K Eldomery, Jacquelyn Reuther, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
November 1, 2014
BCOR-CCNB3 fusions are frequent in undifferentiated sarcomas of male children
Tricia L Peters, Vijetha Kumar, Sumanth Polikepahad, et al.
Human Mutation
|
October 13, 2018
Adapting crowdsourced clinical cancer curation in CIViC to the ClinGen minimum variant level data community-driven standards
Arpad M Danos, Deborah I Ritter, Alex H Wagner, et al.
Pediatric Blood & Cancer
|
October 3, 2020
Integrated DNA and RNA sequencing reveals targetable alterations in metastatic pediatric papillary thyroid carcinoma
Samara L Potter, Jacquelyn Reuther, Raghu Chandramohan, et al.
JCO Precision Oncology
|
October 15, 2021
Durable Response to Larotrectinib in a Child With Histologic Diagnosis of Recurrent Disseminated Ependymoma Discovered to Harbor an <i>NTRK2</i> Fusion: The Impact of Integrated Genomic Profiling
Ross Mangum, Jacquelyn Reuther, Kelsey C Bertrand, et al.
Cancer Genetics
|
February 22, 2025
Anaplastic meningioma in a 6-year-old with somatic YAP1::MAML2 fusion and multiple endocrine neoplasia type 4 (MEN4) syndrome
Lauren R Desrosiers-Battu, John H Lee, Izabela Tarasiewicz, et al.
Page
of 10