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Journal of the National Cancer Institute
|
September 29, 2022
Cancer risks by sex and variant type in PTEN hamartoma tumor syndrome
Linda A J Hendricks, Nicoline Hoogerbrugge, Arjen R Mensenkamp, et al.
Orphanet Journal of Rare Diseases
|
April 29, 2019
The natural history of classic galactosemia: lessons from the GalNet registry
M E Rubio-Gozalbo, M Haskovic, A M Bosch, et al.
American Journal of Human Genetics
|
July 30, 2019
De Novo Heterozygous POLR2A Variants Cause a Neurodevelopmental Syndrome with Profound Infantile-Onset Hypotonia
Hanneke A Haijes, Maria J E Koster, Holger Rehmann, et al.
Nature Communications
|
July 6, 2021
Monocyte-driven atypical cytokine storm and aberrant neutrophil activation as key mediators of COVID-19 disease severity
L Vanderbeke, P Van Mol, Y Van Herck, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 28, 2025
The risk of a second primary cancer in PTEN Hamartoma Tumor Syndrome (PHTS)
Linda A J Hendricks, Katja C J Verbeek, Janneke H M Schuurs-Hoeijmakers, et al.
Cancer Cell
|
February 13, 2019
Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype
Judith E Grolleman, Richarda M de Voer, Fadwa A Elsayed, et al.
Biorxiv : the Preprint Server for Biology
|
September 11, 2024
Brain Charts for the Rhesus Macaque Lifespan
S Alldritt, J S B Ramirez, R Vos de Wael, et al.
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Search research articles
Search
Showing results (261-270 of 267) with videos related to
Sort By:
Page
of 27
You have reached the last page of results.
This site can display upto 267 results.
Journal of the National Cancer Institute
|
September 29, 2022
Cancer risks by sex and variant type in PTEN hamartoma tumor syndrome
Linda A J Hendricks, Nicoline Hoogerbrugge, Arjen R Mensenkamp, et al.
Orphanet Journal of Rare Diseases
|
April 29, 2019
The natural history of classic galactosemia: lessons from the GalNet registry
M E Rubio-Gozalbo, M Haskovic, A M Bosch, et al.
American Journal of Human Genetics
|
July 30, 2019
De Novo Heterozygous POLR2A Variants Cause a Neurodevelopmental Syndrome with Profound Infantile-Onset Hypotonia
Hanneke A Haijes, Maria J E Koster, Holger Rehmann, et al.
Nature Communications
|
July 6, 2021
Monocyte-driven atypical cytokine storm and aberrant neutrophil activation as key mediators of COVID-19 disease severity
L Vanderbeke, P Van Mol, Y Van Herck, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 28, 2025
The risk of a second primary cancer in PTEN Hamartoma Tumor Syndrome (PHTS)
Linda A J Hendricks, Katja C J Verbeek, Janneke H M Schuurs-Hoeijmakers, et al.
Cancer Cell
|
February 13, 2019
Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype
Judith E Grolleman, Richarda M de Voer, Fadwa A Elsayed, et al.
Biorxiv : the Preprint Server for Biology
|
September 11, 2024
Brain Charts for the Rhesus Macaque Lifespan
S Alldritt, J S B Ramirez, R Vos de Wael, et al.
Page
of 27