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Science (New York, N.Y.)
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June 30, 2012
Landscape of somatic retrotransposition in human cancers
Eunjung Lee, Rebecca Iskow, Lixing Yang, et al.
Vaccines
|
August 28, 2021
Changing Attitudes toward the COVID-19 Vaccine among North Carolina Participants in the COVID-19 Community Research Partnership
Chukwunyelu H Enwezor, James E Peacock, Austin L Seals, et al.
Nature
|
September 3, 2010
Integrating common and rare genetic variation in diverse human populations
, David M Altshuler, Richard A Gibbs, et al.
Science Translational Medicine
|
June 17, 2011
Whole-genome sequencing for optimized patient management
Matthew N Bainbridge, Wojciech Wiszniewski, David R Murdock, et al.
Virus Evolution
|
February 16, 2024
Inter and intra-host diversity of RSV in hematopoietic stem cell transplant adults with normal and delayed viral clearance
Vasanthi Avadhanula, Daniel Paiva Agustinho, Vipin Kumar Menon, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 17, 2014
Whole-exome sequencing identifies homozygous GPR161 mutation in a family with pituitary stalk interruption syndrome
Ender Karaca, Ramazan Buyukkaya, Davut Pehlivan, et al.
Children (Basel, Switzerland)
|
May 27, 2026
Echocardiographic Detection of Pulmonary Hypertension and Right Ventricular Failure in Infants with Bronchopulmonary Dysplasia: A Survey of the BPD Collaborative
Shilpa Vyas-Read, Shazia Bhombal, Roopa Siddaiah, et al.
NPJ Microgravity
|
May 14, 2025
The GENESTAR manual for biospecimen collection biobanking and omics data generation from commercial space missions
Aparna Krishnavajhala, Marie-Claude Gingras, Emmanuel Urquieta, et al.
Human Mutation
|
March 1, 2021
Phenotypic and protein localization heterogeneity associated with AHDC1 pathogenic protein-truncating alleles in Xia-Gibbs syndrome
Michael M Khayat, He Li, Varuna Chander, et al.
American Journal of Medical Genetics. Part A
|
November 24, 2021
Quantitative dissection of multilocus pathogenic variation in an Egyptian infant with severe neurodevelopmental disorder resulting from multiple molecular diagnoses
Isabella Herman, Angad Jolly, Haowei Du, et al.
Page
of 117
Search research articles
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Showing results (761-770 of 1,165) with videos related to
Sort By:
Page
of 117
Science (New York, N.Y.)
|
June 30, 2012
Landscape of somatic retrotransposition in human cancers
Eunjung Lee, Rebecca Iskow, Lixing Yang, et al.
Vaccines
|
August 28, 2021
Changing Attitudes toward the COVID-19 Vaccine among North Carolina Participants in the COVID-19 Community Research Partnership
Chukwunyelu H Enwezor, James E Peacock, Austin L Seals, et al.
Nature
|
September 3, 2010
Integrating common and rare genetic variation in diverse human populations
, David M Altshuler, Richard A Gibbs, et al.
Science Translational Medicine
|
June 17, 2011
Whole-genome sequencing for optimized patient management
Matthew N Bainbridge, Wojciech Wiszniewski, David R Murdock, et al.
Virus Evolution
|
February 16, 2024
Inter and intra-host diversity of RSV in hematopoietic stem cell transplant adults with normal and delayed viral clearance
Vasanthi Avadhanula, Daniel Paiva Agustinho, Vipin Kumar Menon, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 17, 2014
Whole-exome sequencing identifies homozygous GPR161 mutation in a family with pituitary stalk interruption syndrome
Ender Karaca, Ramazan Buyukkaya, Davut Pehlivan, et al.
Children (Basel, Switzerland)
|
May 27, 2026
Echocardiographic Detection of Pulmonary Hypertension and Right Ventricular Failure in Infants with Bronchopulmonary Dysplasia: A Survey of the BPD Collaborative
Shilpa Vyas-Read, Shazia Bhombal, Roopa Siddaiah, et al.
NPJ Microgravity
|
May 14, 2025
The GENESTAR manual for biospecimen collection biobanking and omics data generation from commercial space missions
Aparna Krishnavajhala, Marie-Claude Gingras, Emmanuel Urquieta, et al.
Human Mutation
|
March 1, 2021
Phenotypic and protein localization heterogeneity associated with AHDC1 pathogenic protein-truncating alleles in Xia-Gibbs syndrome
Michael M Khayat, He Li, Varuna Chander, et al.
American Journal of Medical Genetics. Part A
|
November 24, 2021
Quantitative dissection of multilocus pathogenic variation in an Egyptian infant with severe neurodevelopmental disorder resulting from multiple molecular diagnoses
Isabella Herman, Angad Jolly, Haowei Du, et al.
Page
of 117