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Journal of the National Comprehensive Cancer Network : JNCCN
|
April 9, 2025
NCCN Guidelines® Insights: Testicular Cancer, Version 2.2025
Timothy Gilligan, Daniel W Lin, Nabil Adra, et al.
Journal of the National Comprehensive Cancer Network : JNCCN
|
September 5, 2024
Cancer-Associated Venous Thromboembolic Disease, Version 2.2024, NCCN Clinical Practice Guidelines in Oncology
Michael B Streiff, Bjorn Holmstrom, Dana Angelini, et al.
Journal of the National Comprehensive Cancer Network : JNCCN
|
August 7, 2023
Adolescent and Young Adult (AYA) Oncology, Version 2.2024, NCCN Clinical Practice Guidelines in Oncology
Smita Bhatia, Alberto S Pappo, Melissa Acquazzino, et al.
Journal of the National Comprehensive Cancer Network : JNCCN
|
April 9, 2026
NCCN Guidelines® Insights: Distress Management, Version 1.2026
Jesse R Fann, Jessica Vanderlan, Benjamin W Brewer, et al.
Journal of the National Comprehensive Cancer Network : JNCCN
|
February 11, 2026
Hodgkin Lymphoma, Version 1.2026, NCCN Clinical Practice Guidelines In Oncology
Ranjana H Advani, Christopher R Kelsey, Philippe Armand, et al.
Neurology
|
March 22, 2022
Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With <i>KCNC2</i> Pathogenic Variants
Niklas Schwarz, Simone Seiffert, Manuela Pendziwiat, et al.
Journal of the National Comprehensive Cancer Network : JNCCN
|
February 12, 2025
NCCN Guidelines® Insights: Head and Neck Cancers, Version 2.2025
A Dimitrios Colevas, Anthony J Cmelak, David G Pfister, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 7, 2021
Haploinsufficiency of PRR12 causes a spectrum of neurodevelopmental, eye, and multisystem abnormalities
Fuad Chowdhury, Lei Wang, Mohammed Al-Raqad, et al.
American Journal of Human Genetics
|
December 31, 2022
Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotype
Susan M Hiatt, Slavica Trajkova, Matteo Rossi Sebastiano, et al.
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Search research articles
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Showing results (21-30 of 29) with videos related to
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You have reached the last page of results.
This site can display upto 29 results.
Journal of the National Comprehensive Cancer Network : JNCCN
|
April 9, 2025
NCCN Guidelines® Insights: Testicular Cancer, Version 2.2025
Timothy Gilligan, Daniel W Lin, Nabil Adra, et al.
Journal of the National Comprehensive Cancer Network : JNCCN
|
September 5, 2024
Cancer-Associated Venous Thromboembolic Disease, Version 2.2024, NCCN Clinical Practice Guidelines in Oncology
Michael B Streiff, Bjorn Holmstrom, Dana Angelini, et al.
Journal of the National Comprehensive Cancer Network : JNCCN
|
August 7, 2023
Adolescent and Young Adult (AYA) Oncology, Version 2.2024, NCCN Clinical Practice Guidelines in Oncology
Smita Bhatia, Alberto S Pappo, Melissa Acquazzino, et al.
Journal of the National Comprehensive Cancer Network : JNCCN
|
April 9, 2026
NCCN Guidelines® Insights: Distress Management, Version 1.2026
Jesse R Fann, Jessica Vanderlan, Benjamin W Brewer, et al.
Journal of the National Comprehensive Cancer Network : JNCCN
|
February 11, 2026
Hodgkin Lymphoma, Version 1.2026, NCCN Clinical Practice Guidelines In Oncology
Ranjana H Advani, Christopher R Kelsey, Philippe Armand, et al.
Neurology
|
March 22, 2022
Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With <i>KCNC2</i> Pathogenic Variants
Niklas Schwarz, Simone Seiffert, Manuela Pendziwiat, et al.
Journal of the National Comprehensive Cancer Network : JNCCN
|
February 12, 2025
NCCN Guidelines® Insights: Head and Neck Cancers, Version 2.2025
A Dimitrios Colevas, Anthony J Cmelak, David G Pfister, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 7, 2021
Haploinsufficiency of PRR12 causes a spectrum of neurodevelopmental, eye, and multisystem abnormalities
Fuad Chowdhury, Lei Wang, Mohammed Al-Raqad, et al.
American Journal of Human Genetics
|
December 31, 2022
Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotype
Susan M Hiatt, Slavica Trajkova, Matteo Rossi Sebastiano, et al.
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of 3