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Pediatric Blood & Cancer
|
August 30, 2020
Ode from an aching heart
Shirley M Abraham
Molecular Genetics and Metabolism
|
January 3, 2017
Combined alpha-delta platelet storage pool deficiency is associated with mutations in GFI1B
Carlos R Ferreira, Dong Chen, Shirley M Abraham, et al.
Genes and Immunity
|
April 22, 2025
A scan of pleiotropic immune mediated disease genes identifies novel determinants of baseline FVIII inhibitor status in hemophilia A
Marcio A Almeida, Vincent P Diego, Kevin R Viel, et al.
Genes and Immunity
|
September 25, 2025
Correction: A scan of pleiotropic immune mediated disease genes identifies novel determinants of baseline FVIII inhibitor status in hemophilia A
Marcio A Almeida, Vincent P Diego, Kevin R Viel, et al.
Blood
|
January 29, 2021
Immunodeficiency and bone marrow failure with mosaic and germline TLR8 gain of function
Jahnavi Aluri, Alicia Bach, Saara Kaviany, et al.
American Journal of Human Genetics
|
June 17, 2014
PGM3 mutations cause a congenital disorder of glycosylation with severe immunodeficiency and skeletal dysplasia
Asbjørg Stray-Pedersen, Paul H Backe, Hanne S Sorte, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
Pediatric Blood & Cancer
|
August 30, 2020
Ode from an aching heart
Shirley M Abraham
Molecular Genetics and Metabolism
|
January 3, 2017
Combined alpha-delta platelet storage pool deficiency is associated with mutations in GFI1B
Carlos R Ferreira, Dong Chen, Shirley M Abraham, et al.
Genes and Immunity
|
April 22, 2025
A scan of pleiotropic immune mediated disease genes identifies novel determinants of baseline FVIII inhibitor status in hemophilia A
Marcio A Almeida, Vincent P Diego, Kevin R Viel, et al.
Genes and Immunity
|
September 25, 2025
Correction: A scan of pleiotropic immune mediated disease genes identifies novel determinants of baseline FVIII inhibitor status in hemophilia A
Marcio A Almeida, Vincent P Diego, Kevin R Viel, et al.
Blood
|
January 29, 2021
Immunodeficiency and bone marrow failure with mosaic and germline TLR8 gain of function
Jahnavi Aluri, Alicia Bach, Saara Kaviany, et al.
American Journal of Human Genetics
|
June 17, 2014
PGM3 mutations cause a congenital disorder of glycosylation with severe immunodeficiency and skeletal dysplasia
Asbjørg Stray-Pedersen, Paul H Backe, Hanne S Sorte, et al.
Page
of 1