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Showing results (111-120 of 117) with videos related to

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American Journal of Medical Genetics. Part A|May 17, 2007
Chromosomal microarray analysis (CMA) detects a large X chromosome deletion including FMR1, FMR2, and IDS in a female patient with mental retardationFrank J Probst, Elizabeth R Roeder, Victoria B Enciso, et al.
American Journal of Medical Genetics. Part A|May 9, 2007
Recurrent interstitial deletions of proximal 18q: a new syndrome involving expressive speech delayJannine D Cody, Courtney Sebold, Amtul Malik, et al.
American Journal of Medical Genetics. Part A|June 18, 2009
Narrowing critical regions and determining penetrance for selected 18q- phenotypesJannine D Cody, Patricia L Heard, Analisa C Crandall, et al.
Human Molecular Genetics|August 1, 1997
Linkage analysis of candidate regions for coeliac disease genesR S Houlston, I P Tomlinson, D Ford, et al.
Journal of Medicinal Chemistry|July 21, 2022
Discovery of Potent and Orally Bioavailable Pyridine N-Oxide-Based Factor XIa Inhibitors through Exploiting Nonclassical InteractionsGuozhang Xu, Zhijie Liu, Xinkang Wang, et al.
Cell|January 17, 2026
Human genetics guides the discovery of CARD9 inhibitors with anti-inflammatory activityJason S Rush, Joshua D Wertheimer, Steven D Goldberg, et al.
Journal of Medicinal Chemistry|April 1, 2026
Optimization of Covalent 6-Cyanoquinazoline KRAS<sup>G12C</sup> Inhibitors for the Treatment of Solid TumorsJesse P Waldo, Paul J Krawczuk, Christopher B Kelly, et al.
Pageof 12

Showing results (111-120 of 117) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 117 results.
American Journal of Medical Genetics. Part A|May 17, 2007
Chromosomal microarray analysis (CMA) detects a large X chromosome deletion including FMR1, FMR2, and IDS in a female patient with mental retardationFrank J Probst, Elizabeth R Roeder, Victoria B Enciso, et al.
American Journal of Medical Genetics. Part A|May 9, 2007
Recurrent interstitial deletions of proximal 18q: a new syndrome involving expressive speech delayJannine D Cody, Courtney Sebold, Amtul Malik, et al.
American Journal of Medical Genetics. Part A|June 18, 2009
Narrowing critical regions and determining penetrance for selected 18q- phenotypesJannine D Cody, Patricia L Heard, Analisa C Crandall, et al.
Human Molecular Genetics|August 1, 1997
Linkage analysis of candidate regions for coeliac disease genesR S Houlston, I P Tomlinson, D Ford, et al.
Journal of Medicinal Chemistry|July 21, 2022
Discovery of Potent and Orally Bioavailable Pyridine N-Oxide-Based Factor XIa Inhibitors through Exploiting Nonclassical InteractionsGuozhang Xu, Zhijie Liu, Xinkang Wang, et al.
Cell|January 17, 2026
Human genetics guides the discovery of CARD9 inhibitors with anti-inflammatory activityJason S Rush, Joshua D Wertheimer, Steven D Goldberg, et al.
Journal of Medicinal Chemistry|April 1, 2026
Optimization of Covalent 6-Cyanoquinazoline KRAS<sup>G12C</sup> Inhibitors for the Treatment of Solid TumorsJesse P Waldo, Paul J Krawczuk, Christopher B Kelly, et al.
Pageof 12