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European Journal of Human Genetics : EJHG
|
February 13, 2014
Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment
Fabiola Ceroni, Nuala H Simpson, Clyde Francks, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 12, 2026
Diagnosis provision by young people's mental health services: a comparison with epidemiological data
Stephanie J Lewis, Alan J Meehan, Mia Akiba, et al.
European Journal of Human Genetics : EJHG
|
August 13, 2002
Refinement of the NHS locus on chromosome Xp22.13 and analysis of five candidate genes
Annick Toutain, Benoît Dessay, Nathalie Ronce, et al.
Plos One
|
December 5, 2012
The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure
Thomas S Scerri, Fahimeh Darki, Dianne F Newbury, et al.
Plos One
|
June 26, 2014
The effectiveness of alcohol screening and brief intervention in emergency departments: a multicentre pragmatic cluster randomized controlled trial
Colin Drummond, Paolo Deluca, Simon Coulton, et al.
Brain : a Journal of Neurology
|
July 14, 2020
SLC12A2 variants cause a neurodevelopmental disorder or cochleovestibular defect
Alisdair McNeill, Emanuela Iovino, Luke Mansard, et al.
Stroke (Hoboken, N.J.)
|
January 26, 2026
Evaluation of an Artificial Intelligence Model for Identification of Intracranial Hemorrhage Subtypes on Computed Tomography of the Head
James M Hillis, Bernardo C Bizzo, Isabella Newbury-Chaet, et al.
Genes, Brain, and Behavior
|
March 18, 2015
Lack of replication for the myosin-18B association with mathematical ability in independent cohorts
K A Pettigrew, S F Fajutrao Valles, K Moll, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 13, 2024
RPL26 variants: A rare cause of Diamond-Blackfan anemia syndrome with multiple congenital anomalies at the forefront
Clémence Vanlerberghe, Frédéric Frénois, Thomas Smol, et al.
Congenital Heart Disease
|
May 1, 2019
Evaluation of Fontan liver disease: Correlation of transjugular liver biopsy with magnetic resonance and hemodynamics
Jose A Silva-Sepulveda, Yudy Fonseca, Irine Vodkin, et al.
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of 83
Search research articles
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Showing results (721-730 of 826) with videos related to
Sort By:
Page
of 83
European Journal of Human Genetics : EJHG
|
February 13, 2014
Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment
Fabiola Ceroni, Nuala H Simpson, Clyde Francks, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 12, 2026
Diagnosis provision by young people's mental health services: a comparison with epidemiological data
Stephanie J Lewis, Alan J Meehan, Mia Akiba, et al.
European Journal of Human Genetics : EJHG
|
August 13, 2002
Refinement of the NHS locus on chromosome Xp22.13 and analysis of five candidate genes
Annick Toutain, Benoît Dessay, Nathalie Ronce, et al.
Plos One
|
December 5, 2012
The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure
Thomas S Scerri, Fahimeh Darki, Dianne F Newbury, et al.
Plos One
|
June 26, 2014
The effectiveness of alcohol screening and brief intervention in emergency departments: a multicentre pragmatic cluster randomized controlled trial
Colin Drummond, Paolo Deluca, Simon Coulton, et al.
Brain : a Journal of Neurology
|
July 14, 2020
SLC12A2 variants cause a neurodevelopmental disorder or cochleovestibular defect
Alisdair McNeill, Emanuela Iovino, Luke Mansard, et al.
Stroke (Hoboken, N.J.)
|
January 26, 2026
Evaluation of an Artificial Intelligence Model for Identification of Intracranial Hemorrhage Subtypes on Computed Tomography of the Head
James M Hillis, Bernardo C Bizzo, Isabella Newbury-Chaet, et al.
Genes, Brain, and Behavior
|
March 18, 2015
Lack of replication for the myosin-18B association with mathematical ability in independent cohorts
K A Pettigrew, S F Fajutrao Valles, K Moll, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 13, 2024
RPL26 variants: A rare cause of Diamond-Blackfan anemia syndrome with multiple congenital anomalies at the forefront
Clémence Vanlerberghe, Frédéric Frénois, Thomas Smol, et al.
Congenital Heart Disease
|
May 1, 2019
Evaluation of Fontan liver disease: Correlation of transjugular liver biopsy with magnetic resonance and hemodynamics
Jose A Silva-Sepulveda, Yudy Fonseca, Irine Vodkin, et al.
Page
of 83