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Journal of the National Cancer Institute
|
May 3, 2024
Identification of TP53 germline variants in pediatric patients undergoing tumor testing: strategy and prevalence
Minjie Luo, Derek Wong, Kristin Zelley, et al.
The Journal of Molecular Diagnostics : JMD
|
December 16, 2023
Uncovering the Genetic Etiology of Inherited Bone Marrow Failure Syndromes Using a Custom-Designed Next-Generation Sequencing Panel
Fumin Lin, Kajia Cao, Fengqi Chang, et al.
Cold Spring Harbor Molecular Case Studies
|
March 2, 2022
A novel <i>TP53</i> tandem duplication in a child with Li-Fraumeni syndrome
Feng Xu, Erfan Aref-Eshghi, Jinhua Wu, et al.
The Journal of Pediatrics
|
July 20, 2023
Comprehensive Gene Panel Testing for Hearing Loss in Children: Understanding Factors Influencing Diagnostic Yield
Nobuko Yamamoto, Jorune Balciuniene, Tiffiney Hartman, et al.
Nature Communications
|
April 7, 2020
Colonic microbiota is associated with inflammation and host epigenomic alterations in inflammatory bowel disease
F J Ryan, A M Ahern, R S Fitzgerald, et al.
Haematologica
|
February 22, 2024
Genomic profiling of pediatric hematologic malignancies and diagnosis of cancer predisposition syndromes: tumoronly <i>versus</i> paired tumor-normal sequencing
Haley Newman, Mary Egan Clark, Derek Wong, et al.
Hemasphere
|
November 27, 2025
Leveraging genomic diagnostics for prognostics and therapeutics in pediatric acute leukemia
Haley Newman, Derek Wong, Jinhua Wu, et al.
Journal of Geophysical Research
|
April 23, 2010
Red tides in the Gulf of Mexico: Where, when, and why?
J J Walsh, J K Jolliff, B P Darrow, et al.
Genome Medicine
|
March 27, 2019
Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome
Francesco Vetrini, Shane McKee, Jill A Rosenfeld, et al.
Genome Medicine
|
March 2, 2019
De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome
Francesco Vetrini, Shane McKee, Jill A Rosenfeld, et al.
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of 12
Search research articles
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Showing results (111-120 of 120) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 120 results.
Journal of the National Cancer Institute
|
May 3, 2024
Identification of TP53 germline variants in pediatric patients undergoing tumor testing: strategy and prevalence
Minjie Luo, Derek Wong, Kristin Zelley, et al.
The Journal of Molecular Diagnostics : JMD
|
December 16, 2023
Uncovering the Genetic Etiology of Inherited Bone Marrow Failure Syndromes Using a Custom-Designed Next-Generation Sequencing Panel
Fumin Lin, Kajia Cao, Fengqi Chang, et al.
Cold Spring Harbor Molecular Case Studies
|
March 2, 2022
A novel <i>TP53</i> tandem duplication in a child with Li-Fraumeni syndrome
Feng Xu, Erfan Aref-Eshghi, Jinhua Wu, et al.
The Journal of Pediatrics
|
July 20, 2023
Comprehensive Gene Panel Testing for Hearing Loss in Children: Understanding Factors Influencing Diagnostic Yield
Nobuko Yamamoto, Jorune Balciuniene, Tiffiney Hartman, et al.
Nature Communications
|
April 7, 2020
Colonic microbiota is associated with inflammation and host epigenomic alterations in inflammatory bowel disease
F J Ryan, A M Ahern, R S Fitzgerald, et al.
Haematologica
|
February 22, 2024
Genomic profiling of pediatric hematologic malignancies and diagnosis of cancer predisposition syndromes: tumoronly <i>versus</i> paired tumor-normal sequencing
Haley Newman, Mary Egan Clark, Derek Wong, et al.
Hemasphere
|
November 27, 2025
Leveraging genomic diagnostics for prognostics and therapeutics in pediatric acute leukemia
Haley Newman, Derek Wong, Jinhua Wu, et al.
Journal of Geophysical Research
|
April 23, 2010
Red tides in the Gulf of Mexico: Where, when, and why?
J J Walsh, J K Jolliff, B P Darrow, et al.
Genome Medicine
|
March 27, 2019
Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome
Francesco Vetrini, Shane McKee, Jill A Rosenfeld, et al.
Genome Medicine
|
March 2, 2019
De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome
Francesco Vetrini, Shane McKee, Jill A Rosenfeld, et al.
Page
of 12