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David Traver

Showing results (111-120 of 115) with videos related to

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American Journal of Human Genetics|August 5, 2008
Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndromeVincent Cantagrel, Jennifer L Silhavy, Stephanie L Bielas, et al.
Blood|September 5, 2009
The role and regulation of friend of GATA-1 (FOG-1) during blood development in the zebrafishJulio D Amigo, Gabriele E Ackermann, John J Cope, et al.
Nature Genetics|January 17, 2017
Biallelic mutations in the 3' exonuclease TOE1 cause pontocerebellar hypoplasia and uncover a role in snRNA processingRea M Lardelli, Ashleigh E Schaffer, Veerle R C Eggens, et al.
The New England Journal of Medicine|June 21, 2023
Systemic Inflammation and Normocytic Anemia in DOCK11 DeficiencyJana Block, Christina Rashkova, Irinka Castanon, et al.
American Journal of Human Genetics|August 23, 2016
De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability SyndromeJung-Hyun Kim, Deepali N Shinde, Margot R F Reijnders, et al.
Pageof 12

Showing results (111-120 of 115) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 115 results.
American Journal of Human Genetics|August 5, 2008
Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndromeVincent Cantagrel, Jennifer L Silhavy, Stephanie L Bielas, et al.
Blood|September 5, 2009
The role and regulation of friend of GATA-1 (FOG-1) during blood development in the zebrafishJulio D Amigo, Gabriele E Ackermann, John J Cope, et al.
Nature Genetics|January 17, 2017
Biallelic mutations in the 3' exonuclease TOE1 cause pontocerebellar hypoplasia and uncover a role in snRNA processingRea M Lardelli, Ashleigh E Schaffer, Veerle R C Eggens, et al.
The New England Journal of Medicine|June 21, 2023
Systemic Inflammation and Normocytic Anemia in DOCK11 DeficiencyJana Block, Christina Rashkova, Irinka Castanon, et al.
American Journal of Human Genetics|August 23, 2016
De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability SyndromeJung-Hyun Kim, Deepali N Shinde, Margot R F Reijnders, et al.
Pageof 12