Search research articles
Contact Us
Filters
Showing results (21-30 of 26) with videos related to
Page
of 3
Sort By:
You have reached the last page of results.
This site can display upto 26 results.
American Journal of Human Genetics
|
April 17, 2018
Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia
Claire Guissart, Xenia Latypova, Paul Rollier, et al.
Brain : a Journal of Neurology
|
April 6, 2017
Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders
Markus Wolff, Katrine M Johannesen, Ulrike B S Hedrich, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 4, 2020
NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns
Hannah Stamberger, Trine B Hammer, Elena Gardella, et al.
Nature Communications
|
February 1, 2020
Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy
Holger Hengel, Célia Bosso-Lefèvre, George Grady, et al.
Molecular Psychiatry
|
November 17, 2022
Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition
Elizabeth E Palmer, Michael Pusch, Alessandra Picollo, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 3, 2023
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes
Siwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 26) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 26 results.
American Journal of Human Genetics
|
April 17, 2018
Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia
Claire Guissart, Xenia Latypova, Paul Rollier, et al.
Brain : a Journal of Neurology
|
April 6, 2017
Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders
Markus Wolff, Katrine M Johannesen, Ulrike B S Hedrich, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 4, 2020
NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns
Hannah Stamberger, Trine B Hammer, Elena Gardella, et al.
Nature Communications
|
February 1, 2020
Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy
Holger Hengel, Célia Bosso-Lefèvre, George Grady, et al.
Molecular Psychiatry
|
November 17, 2022
Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition
Elizabeth E Palmer, Michael Pusch, Alessandra Picollo, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 3, 2023
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes
Siwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.
Page
of 3