Search research articles
Contact Us
Filters
Showing results (21-30 of 25) with videos related to
Page
of 3
Sort By:
You have reached the last page of results.
This site can display upto 25 results.
ACS Sensors
|
August 23, 2023
Multiplexed Biosensing of Proteins and Virions with Disposable Plasmonic Assays
Stephanie Wallace, Martin Kartau, Tarun Kakkar, et al.
Vaccines
|
January 28, 2026
Booster Immunisation with Skin-Patch-Delivered Unadjuvanted SARS-CoV-2 Spike Protein Vaccine Is Safe and Immunogenic in Healthy Adults
Christopher L D McMillan, David A Muller, Germain J P Fernando, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 3, 2010
Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity
Ruxandra Bachmann-Gagescu, Heather C Mefford, Charles Cowan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 3, 2019
The pleiotropy associated with de novo variants in CHD4, CNOT3, and SETD5 extends to moyamoya angiopathy
Amélie Pinard, Stéphanie Guey, Dongchuan Guo, et al.
Human Mutation
|
July 17, 2015
High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype-Phenotype Correlation
Kitiwan Rojnueangnit, Jing Xie, Alicia Gomes, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 25) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 25 results.
ACS Sensors
|
August 23, 2023
Multiplexed Biosensing of Proteins and Virions with Disposable Plasmonic Assays
Stephanie Wallace, Martin Kartau, Tarun Kakkar, et al.
Vaccines
|
January 28, 2026
Booster Immunisation with Skin-Patch-Delivered Unadjuvanted SARS-CoV-2 Spike Protein Vaccine Is Safe and Immunogenic in Healthy Adults
Christopher L D McMillan, David A Muller, Germain J P Fernando, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 3, 2010
Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity
Ruxandra Bachmann-Gagescu, Heather C Mefford, Charles Cowan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 3, 2019
The pleiotropy associated with de novo variants in CHD4, CNOT3, and SETD5 extends to moyamoya angiopathy
Amélie Pinard, Stéphanie Guey, Dongchuan Guo, et al.
Human Mutation
|
July 17, 2015
High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype-Phenotype Correlation
Kitiwan Rojnueangnit, Jing Xie, Alicia Gomes, et al.
Page
of 3