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Plos One
|
September 5, 2008
Small deletion variants have stable breakpoints commonly associated with alu elements
Adam J de Smith, Robin G Walters, Lachlan J M Coin, et al.
HGG Advances
|
September 15, 2023
Evaluating genomic polygenic risk scores for childhood acute lymphoblastic leukemia in Latinos
Soyoung Jeon, Ying Chu Lo, Libby M Morimoto, et al.
Blood
|
November 9, 2013
GATA3 risk alleles are associated with ancestral components in Hispanic children with ALL
Kyle M Walsh, Adam J de Smith, Anand P Chokkalingam, et al.
Neuro-Oncology Advances
|
May 16, 2022
Mitochondrial 1555 G>A variant as a potential risk factor for childhood glioblastoma
Shaobo Li, Xiaowu Gai, Swe Swe Myint, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 24, 2025
Hypothesis-generating analysis of mutational signatures in childhood B-cell acute lymphoblastic leukemia in relation to socio-demographic, genetic, and environmental factors: A report from the Children's Oncology Group
Cassandra J Clark, Zhanni Lu, Nathan Anderson, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 3, 2023
Evaluating Genomic Polygenic Risk Scores for Childhood Acute Lymphoblastic Leukemia in Latinos
Soyoung Jeon, Ying Chu Lo, Libby M Morimoto, et al.
Blood Advances
|
February 22, 2020
Germline variants in predisposition genes in children with Down syndrome and acute lymphoblastic leukemia
Peleg Winer, Ivo S Muskens, Kyle M Walsh, et al.
Neuro-Oncology Advances
|
September 1, 2020
Pediatric glioma and medulloblastoma risk and population demographics: a Poisson regression analysis
Ivo S Muskens, Qianxi Feng, Stephen S Francis, et al.
Neuro-Oncology
|
January 24, 2020
Germline cancer predisposition variants and pediatric glioma: a population-based study in California
Ivo S Muskens, Adam J de Smith, Chenan Zhang, et al.
Human Molecular Genetics
|
December 24, 2013
Imprinted expression of UBE3A in non-neuronal cells from a Prader-Willi syndrome patient with an atypical deletion
Kristen Martins-Taylor, Jack S Hsiao, Pin-Fang Chen, et al.
Page
of 11
Search research articles
Search
Showing results (21-30 of 106) with videos related to
Sort By:
Page
of 11
Plos One
|
September 5, 2008
Small deletion variants have stable breakpoints commonly associated with alu elements
Adam J de Smith, Robin G Walters, Lachlan J M Coin, et al.
HGG Advances
|
September 15, 2023
Evaluating genomic polygenic risk scores for childhood acute lymphoblastic leukemia in Latinos
Soyoung Jeon, Ying Chu Lo, Libby M Morimoto, et al.
Blood
|
November 9, 2013
GATA3 risk alleles are associated with ancestral components in Hispanic children with ALL
Kyle M Walsh, Adam J de Smith, Anand P Chokkalingam, et al.
Neuro-Oncology Advances
|
May 16, 2022
Mitochondrial 1555 G>A variant as a potential risk factor for childhood glioblastoma
Shaobo Li, Xiaowu Gai, Swe Swe Myint, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 24, 2025
Hypothesis-generating analysis of mutational signatures in childhood B-cell acute lymphoblastic leukemia in relation to socio-demographic, genetic, and environmental factors: A report from the Children's Oncology Group
Cassandra J Clark, Zhanni Lu, Nathan Anderson, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 3, 2023
Evaluating Genomic Polygenic Risk Scores for Childhood Acute Lymphoblastic Leukemia in Latinos
Soyoung Jeon, Ying Chu Lo, Libby M Morimoto, et al.
Blood Advances
|
February 22, 2020
Germline variants in predisposition genes in children with Down syndrome and acute lymphoblastic leukemia
Peleg Winer, Ivo S Muskens, Kyle M Walsh, et al.
Neuro-Oncology Advances
|
September 1, 2020
Pediatric glioma and medulloblastoma risk and population demographics: a Poisson regression analysis
Ivo S Muskens, Qianxi Feng, Stephen S Francis, et al.
Neuro-Oncology
|
January 24, 2020
Germline cancer predisposition variants and pediatric glioma: a population-based study in California
Ivo S Muskens, Adam J de Smith, Chenan Zhang, et al.
Human Molecular Genetics
|
December 24, 2013
Imprinted expression of UBE3A in non-neuronal cells from a Prader-Willi syndrome patient with an atypical deletion
Kristen Martins-Taylor, Jack S Hsiao, Pin-Fang Chen, et al.
Page
of 11