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International Journal of Experimental Pathology
|
June 13, 2002
Heterogeneity in the granulomatous response to mycobacterial infection in patients with defined genetic mutations in the interleukin 12-dependent interferon-gamma production pathway
David A Lammas, E De Heer, J D Edgar, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
November 20, 2012
The capsular polysaccharide Vi from Salmonella typhi is a B1b antigen
Jennifer L Marshall, Adriana Flores-Langarica, Robert A Kingsley, et al.
Human Mutation
|
May 24, 2022
De novo truncating NOVA2 variants affect alternative splicing and lead to heterogeneous neurodevelopmental phenotypes
Marcello Scala, Nathalie Drouot, Suzanna C MacLennan, et al.
Human Mutation
|
October 30, 2019
Recurrent TTN metatranscript-only c.39974-11T>G splice variant associated with autosomal recessive arthrogryposis multiplex congenita and myopathy
Samantha J Bryen, Lisa J Ewans, Jason Pinner, et al.
Nature Genetics
|
September 29, 2020
Mutations disrupting neuritogenesis genes confer risk for cerebral palsy
Sheng Chih Jin, Sara A Lewis, Somayeh Bakhtiari, et al.
Page
of 16
Search research articles
Search
Showing results (151-160 of 155) with videos related to
Sort By:
Page
of 16
You have reached the last page of results.
This site can display upto 155 results.
International Journal of Experimental Pathology
|
June 13, 2002
Heterogeneity in the granulomatous response to mycobacterial infection in patients with defined genetic mutations in the interleukin 12-dependent interferon-gamma production pathway
David A Lammas, E De Heer, J D Edgar, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
November 20, 2012
The capsular polysaccharide Vi from Salmonella typhi is a B1b antigen
Jennifer L Marshall, Adriana Flores-Langarica, Robert A Kingsley, et al.
Human Mutation
|
May 24, 2022
De novo truncating NOVA2 variants affect alternative splicing and lead to heterogeneous neurodevelopmental phenotypes
Marcello Scala, Nathalie Drouot, Suzanna C MacLennan, et al.
Human Mutation
|
October 30, 2019
Recurrent TTN metatranscript-only c.39974-11T>G splice variant associated with autosomal recessive arthrogryposis multiplex congenita and myopathy
Samantha J Bryen, Lisa J Ewans, Jason Pinner, et al.
Nature Genetics
|
September 29, 2020
Mutations disrupting neuritogenesis genes confer risk for cerebral palsy
Sheng Chih Jin, Sara A Lewis, Somayeh Bakhtiari, et al.
Page
of 16