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Neurogenetics
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February 16, 2005
A novel NIPA1 mutation associated with a pure form of autosomal dominant hereditary spastic paraplegia
Johanna A Reed, Phillip A Wilkinson, Heema Patel, et al.
Magnetic Resonance Annual
|
January 1, 1985
Principles of magnetic resonance
J P Jones, C L Partain, M R Mitchell, et al.
ACS Nano
|
September 1, 2018
Cation-Activated Avidity for Rapid Reconfiguration of DNA Nanodevices
Alexander E Marras, Ze Shi, Michael G Lindell, et al.
European Journal of Human Genetics : EJHG
|
December 31, 1997
Further delineation of the critical region for noonan syndrome on the long arm of chromosome 12
A F Brady, C R Jamieson, I van der Burgt, et al.
Journal of Racial and Ethnic Health Disparities
|
October 7, 2025
Disparities in Stage at Diagnosis and Cancer Progression by Race and Socioeconomic Deprivation: A Pan-Tumor Analysis in the US Community Oncology Setting
Andrew J Osterland, Yunfei Wang, Esther R Smith-Howell, et al.
Human Genetics
|
May 8, 2000
Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22
A R Afzal, A Rajab, C Fenske, et al.
Orthopaedic Journal of Sports Medicine
|
March 19, 2021
Sport- and Gender-Based Differences in Head Impact Exposure and Mechanism in High School Sports
Colin M Huber, Declan A Patton, Catherine C McDonald, et al.
Journal of Human Genetics
|
February 4, 2005
Genetic heterogeneity in LEOPARD syndrome: two families with no mutations in PTPN11
Kamini Kalidas, Adam C Shaw, Andrew H Crosby, et al.
Nature Genetics
|
December 1, 1994
Mapping a gene for Noonan syndrome to the long arm of chromosome 12
C R Jamieson, I van der Burgt, A F Brady, et al.
The Protein Journal
|
November 15, 2006
The effects of removing the GAT domain from E. coli GMP synthetase
Jessica L Abbott, Jordan M Newell, Christine M Lightcap, et al.
Page
of 42
Search research articles
Search
Showing results (341-350 of 412) with videos related to
Sort By:
Page
of 42
Neurogenetics
|
February 16, 2005
A novel NIPA1 mutation associated with a pure form of autosomal dominant hereditary spastic paraplegia
Johanna A Reed, Phillip A Wilkinson, Heema Patel, et al.
Magnetic Resonance Annual
|
January 1, 1985
Principles of magnetic resonance
J P Jones, C L Partain, M R Mitchell, et al.
ACS Nano
|
September 1, 2018
Cation-Activated Avidity for Rapid Reconfiguration of DNA Nanodevices
Alexander E Marras, Ze Shi, Michael G Lindell, et al.
European Journal of Human Genetics : EJHG
|
December 31, 1997
Further delineation of the critical region for noonan syndrome on the long arm of chromosome 12
A F Brady, C R Jamieson, I van der Burgt, et al.
Journal of Racial and Ethnic Health Disparities
|
October 7, 2025
Disparities in Stage at Diagnosis and Cancer Progression by Race and Socioeconomic Deprivation: A Pan-Tumor Analysis in the US Community Oncology Setting
Andrew J Osterland, Yunfei Wang, Esther R Smith-Howell, et al.
Human Genetics
|
May 8, 2000
Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22
A R Afzal, A Rajab, C Fenske, et al.
Orthopaedic Journal of Sports Medicine
|
March 19, 2021
Sport- and Gender-Based Differences in Head Impact Exposure and Mechanism in High School Sports
Colin M Huber, Declan A Patton, Catherine C McDonald, et al.
Journal of Human Genetics
|
February 4, 2005
Genetic heterogeneity in LEOPARD syndrome: two families with no mutations in PTPN11
Kamini Kalidas, Adam C Shaw, Andrew H Crosby, et al.
Nature Genetics
|
December 1, 1994
Mapping a gene for Noonan syndrome to the long arm of chromosome 12
C R Jamieson, I van der Burgt, A F Brady, et al.
The Protein Journal
|
November 15, 2006
The effects of removing the GAT domain from E. coli GMP synthetase
Jessica L Abbott, Jordan M Newell, Christine M Lightcap, et al.
Page
of 42