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Neuropathology and Applied Neurobiology
|
March 15, 2024
Atypical teratoid/rhabdoid tumour-TYR subtype arising in the setting of germline ring chromosome 22: An uncommon form of tumour predisposition
Julieann C Lee, Quynh T Tran, Rose B McGee, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
September 25, 2024
Update on Surveillance for Wilms Tumor and Hepatoblastoma in Beckwith-Wiedemann Syndrome and Other Predisposition Syndromes
Jennifer M Kalish, Kerri D Becktell, Gaëlle Bougeard, et al.
American Journal of Medical Genetics. Part A
|
February 6, 2019
Hyperinsulinemic hypoglycemia in seven patients with de novo NSD1 mutations
Katheryn Grand, Christina Gonzalez-Gandolfi, Amanda M Ackermann, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
June 11, 2024
Clinical Updates and Surveillance Recommendations for DNA Replication Repair Deficiency Syndromes in Children and Young Adults
Anirban Das, Suzanne P MacFarland, Julia Meade, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
February 12, 2025
Update on Cancer and Central Nervous System Tumor Surveillance in Pediatric NF2-, SMARCB1-, and LZTR1-Related Schwannomatosis
Melissa R Perrino, Marjolijn C J Jongmans, Gail E Tomlinson, et al.
Pediatrics
|
June 1, 2022
Clinical Effectiveness of Telemedicine-Based Pediatric Genetics Care
Katherine M Szigety, Terrence B Crowley, Kimberly B Gaiser, et al.
Cancer
|
April 23, 2020
11p15.5 epimutations in children with Wilms tumor and hepatoblastoma detected in peripheral blood
Elise M Fiala, Michael V Ortiz, Jennifer A Kennedy, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
August 28, 2024
Update on Pediatric Cancer Surveillance Recommendations for Patients with Neurofibromatosis Type 1, Noonan Syndrome, CBL Syndrome, Costello Syndrome, and Related RASopathies
Melissa R Perrino, Anirban Das, Sarah R Scollon, et al.
Clinical Epigenetics
|
August 1, 2024
Multi-locus imprinting disturbance (MLID): interim joint statement for clinical and molecular diagnosis
Deborah J G Mackay, Gabriella Gazdagh, David Monk, et al.
Nature Reviews. Endocrinology
|
January 30, 2018
Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement
Frédéric Brioude, Jennifer M Kalish, Alessandro Mussa, et al.
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Search research articles
Search
Showing results (101-110 of 112) with videos related to
Sort By:
Page
of 12
Neuropathology and Applied Neurobiology
|
March 15, 2024
Atypical teratoid/rhabdoid tumour-TYR subtype arising in the setting of germline ring chromosome 22: An uncommon form of tumour predisposition
Julieann C Lee, Quynh T Tran, Rose B McGee, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
September 25, 2024
Update on Surveillance for Wilms Tumor and Hepatoblastoma in Beckwith-Wiedemann Syndrome and Other Predisposition Syndromes
Jennifer M Kalish, Kerri D Becktell, Gaëlle Bougeard, et al.
American Journal of Medical Genetics. Part A
|
February 6, 2019
Hyperinsulinemic hypoglycemia in seven patients with de novo NSD1 mutations
Katheryn Grand, Christina Gonzalez-Gandolfi, Amanda M Ackermann, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
June 11, 2024
Clinical Updates and Surveillance Recommendations for DNA Replication Repair Deficiency Syndromes in Children and Young Adults
Anirban Das, Suzanne P MacFarland, Julia Meade, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
February 12, 2025
Update on Cancer and Central Nervous System Tumor Surveillance in Pediatric NF2-, SMARCB1-, and LZTR1-Related Schwannomatosis
Melissa R Perrino, Marjolijn C J Jongmans, Gail E Tomlinson, et al.
Pediatrics
|
June 1, 2022
Clinical Effectiveness of Telemedicine-Based Pediatric Genetics Care
Katherine M Szigety, Terrence B Crowley, Kimberly B Gaiser, et al.
Cancer
|
April 23, 2020
11p15.5 epimutations in children with Wilms tumor and hepatoblastoma detected in peripheral blood
Elise M Fiala, Michael V Ortiz, Jennifer A Kennedy, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
August 28, 2024
Update on Pediatric Cancer Surveillance Recommendations for Patients with Neurofibromatosis Type 1, Noonan Syndrome, CBL Syndrome, Costello Syndrome, and Related RASopathies
Melissa R Perrino, Anirban Das, Sarah R Scollon, et al.
Clinical Epigenetics
|
August 1, 2024
Multi-locus imprinting disturbance (MLID): interim joint statement for clinical and molecular diagnosis
Deborah J G Mackay, Gabriella Gazdagh, David Monk, et al.
Nature Reviews. Endocrinology
|
January 30, 2018
Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement
Frédéric Brioude, Jennifer M Kalish, Alessandro Mussa, et al.
Page
of 12