Search research articles
Contact Us
Filters
Showing results (21-30 of 25) with videos related to
Page
of 3
Sort By:
You have reached the last page of results.
This site can display upto 25 results.
Neuron
|
August 5, 2003
Local tissue interactions across the dorsal midline of the forebrain establish CNS laterality
Miguel L Concha, Claire Russell, Jennifer C Regan, et al.
Nature Communications
|
July 29, 2025
Autocrine interferon poisoning mediates ADAR1-dependent synthetic lethality in BRCA1/2-mutant cancers
Roman M Chabanon, Liudmila Shcherbakova, Magali Lacroix-Triki, et al.
American Journal of Human Genetics
|
February 5, 2026
Bi-allelic loss-of-function variants in JKAMP cause a neurodevelopmental syndrome associated with dysregulation of GPR37 trafficking
Pilar Chacon-Millan, Antonella Delicato, Arif Mahmood, et al.
Human Molecular Genetics
|
December 10, 2013
Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects
Annie Laquérriere, Jérome Maluenda, Adrien Camus, et al.
Journal of Medical Genetics
|
April 6, 2021
Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita
Annie Laquerriere, Dana Jaber, Emanuela Abiusi, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 25) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 25 results.
Neuron
|
August 5, 2003
Local tissue interactions across the dorsal midline of the forebrain establish CNS laterality
Miguel L Concha, Claire Russell, Jennifer C Regan, et al.
Nature Communications
|
July 29, 2025
Autocrine interferon poisoning mediates ADAR1-dependent synthetic lethality in BRCA1/2-mutant cancers
Roman M Chabanon, Liudmila Shcherbakova, Magali Lacroix-Triki, et al.
American Journal of Human Genetics
|
February 5, 2026
Bi-allelic loss-of-function variants in JKAMP cause a neurodevelopmental syndrome associated with dysregulation of GPR37 trafficking
Pilar Chacon-Millan, Antonella Delicato, Arif Mahmood, et al.
Human Molecular Genetics
|
December 10, 2013
Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects
Annie Laquérriere, Jérome Maluenda, Adrien Camus, et al.
Journal of Medical Genetics
|
April 6, 2021
Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita
Annie Laquerriere, Dana Jaber, Emanuela Abiusi, et al.
Page
of 3