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Haematologica
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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.
Blood Advances
|
August 15, 2025
Role of race and ethnicity in survival among children/young adults with relapsed ALL: a Children's Oncology Group report
John A Ligon, Lingyun Ji, Alice Dang, et al.
Nature Communications
|
July 8, 2025
Inferring chromosome segregation error stage and crossover in trisomic disorders with application to Down syndrome
Zhenhua Li, Wenjian Yang, Gang Wu, et al.
NPJ Genomic Medicine
|
July 11, 2017
The clinical impact of copy number variants in inherited bone marrow failure syndromes
Nicolas Waespe, Santhosh Dhanraj, Manju Wahala, et al.
Cancer Genetics
|
August 20, 2019
Masked hypodiploidy: Hypodiploid acute lymphoblastic leukemia (ALL) mimicking hyperdiploid ALL in children: A report from the Children's Oncology Group
Andrew J Carroll, Mary Shago, Fady M Mikhail, et al.
Scientific Reports
|
July 2, 2016
Indexing Effects of Copy Number Variation on Genes Involved in Developmental Delay
Mohammed Uddin, Giovanna Pellecchia, Bhooma Thiruvahindrapuram, et al.
Blood
|
March 31, 2023
Genomic landscape of Down syndrome-associated acute lymphoblastic leukemia
Zhenhua Li, Ti-Cheng Chang, Jacob J Junco, et al.
JCI Insight
|
May 23, 2022
Hypomorphic GINS3 variants alter DNA replication and cause Meier-Gorlin syndrome
Mary E McQuaid, Kashif Ahmed, Stephanie Tran, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
February 11, 2015
BRAF mutation and CDKN2A deletion define a clinically distinct subgroup of childhood secondary high-grade glioma
Matthew Mistry, Nataliya Zhukova, Daniele Merico, et al.
American Journal of Human Genetics
|
February 7, 2008
Structural variation of chromosomes in autism spectrum disorder
Christian R Marshall, Abdul Noor, John B Vincent, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 69) with videos related to
Sort By:
Page
of 7
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.
Blood Advances
|
August 15, 2025
Role of race and ethnicity in survival among children/young adults with relapsed ALL: a Children's Oncology Group report
John A Ligon, Lingyun Ji, Alice Dang, et al.
Nature Communications
|
July 8, 2025
Inferring chromosome segregation error stage and crossover in trisomic disorders with application to Down syndrome
Zhenhua Li, Wenjian Yang, Gang Wu, et al.
NPJ Genomic Medicine
|
July 11, 2017
The clinical impact of copy number variants in inherited bone marrow failure syndromes
Nicolas Waespe, Santhosh Dhanraj, Manju Wahala, et al.
Cancer Genetics
|
August 20, 2019
Masked hypodiploidy: Hypodiploid acute lymphoblastic leukemia (ALL) mimicking hyperdiploid ALL in children: A report from the Children's Oncology Group
Andrew J Carroll, Mary Shago, Fady M Mikhail, et al.
Scientific Reports
|
July 2, 2016
Indexing Effects of Copy Number Variation on Genes Involved in Developmental Delay
Mohammed Uddin, Giovanna Pellecchia, Bhooma Thiruvahindrapuram, et al.
Blood
|
March 31, 2023
Genomic landscape of Down syndrome-associated acute lymphoblastic leukemia
Zhenhua Li, Ti-Cheng Chang, Jacob J Junco, et al.
JCI Insight
|
May 23, 2022
Hypomorphic GINS3 variants alter DNA replication and cause Meier-Gorlin syndrome
Mary E McQuaid, Kashif Ahmed, Stephanie Tran, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
February 11, 2015
BRAF mutation and CDKN2A deletion define a clinically distinct subgroup of childhood secondary high-grade glioma
Matthew Mistry, Nataliya Zhukova, Daniele Merico, et al.
American Journal of Human Genetics
|
February 7, 2008
Structural variation of chromosomes in autism spectrum disorder
Christian R Marshall, Abdul Noor, John B Vincent, et al.
Page
of 7