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Journal of Medical Genetics
|
June 11, 2011
Genetic analysis of inherited bone marrow failure syndromes from one prospective, comprehensive and population-based cohort and identification of novel mutations
E Tsangaris, R Klaassen, C V Fernandez, et al.
Haematologica
|
February 16, 2015
The impact of category, cytopathology and cytogenetics on development and progression of clonal and malignant myeloid transformation in inherited bone marrow failure syndromes
Michaela Cada, Catherin I Segbefia, Robert Klaassen, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
March 6, 2020
Activity of Vincristine and Irinotecan in Diffuse Anaplastic Wilms Tumor and Therapy Outcomes of Stage II to IV Disease: Results of the Children's Oncology Group AREN0321 Study
Najat C Daw, Yueh-Yun Chi, John A Kalapurakal, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
November 12, 2025
Impact of Pulmonary Tumor Burden in Favorable Histology Wilms Tumor Outcomes: A Report From the Children's Oncology Group Study AREN0533
David B Dix, Geetika Khanna, Lindsay A Renfro, et al.
Nature Communications
|
December 6, 2023
Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD
Sheng Wang, Belinda Wang, Vanessa Drury, et al.
Journal of the American College of Surgeons
|
January 22, 2024
Race and Ethnic Group Enrollment and Outcomes for Wilms Tumor: Analysis of the Current Era Children's Oncology Group Study, AREN03B2
Harold N Lovvorn, Lindsay A Renfro, Daniel J Benedetti, et al.
American Journal of Medical Genetics. Part A
|
October 7, 2008
Molecular characterization of a patient with 3p deletion syndrome and a review of the literature
Thomas V Fernandez, I J García-González, Christopher E Mason, et al.
Annals of Surgery
|
November 5, 2016
Clinical Outcome and Biological Predictors of Relapse After Nephrectomy Only for Very Low-risk Wilms Tumor: A Report From Children's Oncology Group AREN0532
Conrad V Fernandez, Elizabeth J Perlman, Elizabeth A Mullen, et al.
Biorxiv : the Preprint Server for Biology
|
December 25, 2025
The urinary pathobiont <i>Actinobaculum massiliense</i> generates androgens via the <i>dirAB</i> pathway
Taojun Wang, Saeed Ahmad, Raissa Santos de Lima Rosa, et al.
Neuron
|
May 5, 2017
De Novo Coding Variants Are Strongly Associated with Tourette Disorder
A Jeremy Willsey, Thomas V Fernandez, Dongmei Yu, et al.
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Search research articles
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Showing results (441-450 of 597) with videos related to
Sort By:
Page
of 60
Journal of Medical Genetics
|
June 11, 2011
Genetic analysis of inherited bone marrow failure syndromes from one prospective, comprehensive and population-based cohort and identification of novel mutations
E Tsangaris, R Klaassen, C V Fernandez, et al.
Haematologica
|
February 16, 2015
The impact of category, cytopathology and cytogenetics on development and progression of clonal and malignant myeloid transformation in inherited bone marrow failure syndromes
Michaela Cada, Catherin I Segbefia, Robert Klaassen, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
March 6, 2020
Activity of Vincristine and Irinotecan in Diffuse Anaplastic Wilms Tumor and Therapy Outcomes of Stage II to IV Disease: Results of the Children's Oncology Group AREN0321 Study
Najat C Daw, Yueh-Yun Chi, John A Kalapurakal, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
November 12, 2025
Impact of Pulmonary Tumor Burden in Favorable Histology Wilms Tumor Outcomes: A Report From the Children's Oncology Group Study AREN0533
David B Dix, Geetika Khanna, Lindsay A Renfro, et al.
Nature Communications
|
December 6, 2023
Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD
Sheng Wang, Belinda Wang, Vanessa Drury, et al.
Journal of the American College of Surgeons
|
January 22, 2024
Race and Ethnic Group Enrollment and Outcomes for Wilms Tumor: Analysis of the Current Era Children's Oncology Group Study, AREN03B2
Harold N Lovvorn, Lindsay A Renfro, Daniel J Benedetti, et al.
American Journal of Medical Genetics. Part A
|
October 7, 2008
Molecular characterization of a patient with 3p deletion syndrome and a review of the literature
Thomas V Fernandez, I J García-González, Christopher E Mason, et al.
Annals of Surgery
|
November 5, 2016
Clinical Outcome and Biological Predictors of Relapse After Nephrectomy Only for Very Low-risk Wilms Tumor: A Report From Children's Oncology Group AREN0532
Conrad V Fernandez, Elizabeth J Perlman, Elizabeth A Mullen, et al.
Biorxiv : the Preprint Server for Biology
|
December 25, 2025
The urinary pathobiont <i>Actinobaculum massiliense</i> generates androgens via the <i>dirAB</i> pathway
Taojun Wang, Saeed Ahmad, Raissa Santos de Lima Rosa, et al.
Neuron
|
May 5, 2017
De Novo Coding Variants Are Strongly Associated with Tourette Disorder
A Jeremy Willsey, Thomas V Fernandez, Dongmei Yu, et al.
Page
of 60