Search research articles
Contact Us
Filters
Showing results (281-290 of 291) with videos related to
Page
of 30
Sort By:
HGG Advances
|
September 4, 2023
Rare variants in <i>CAPN2</i> increase risk for isolated hypoplastic left heart syndrome
Elizabeth E Blue, Janson J White, Michael K Dush, et al.
Viruses
|
June 11, 2020
Tenth Scientific Biennial Meeting of the Australasian Virology Society-AVS10 2019
Karla J Helbig, Rowena A Bull, Rebecca Ambrose, et al.
Acta Neuropathologica Communications
|
April 8, 2021
Molecular classification of a complex structural rearrangement of the RB1 locus in an infant with sporadic, isolated, intracranial, sellar region retinoblastoma
Kathleen M Schieffer, Alexander Z Feldman, Esko A Kautto, et al.
BMC Genomics
|
December 5, 2021
Discovery of clinically relevant fusions in pediatric cancer
Stephanie LaHaye, James R Fitch, Kyle J Voytovich, et al.
HGG Advances
|
December 10, 2021
Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease
Polakit Teekakirikul, Wenjuan Zhu, George C Gabriel, et al.
Molecular Psychiatry
|
May 6, 2018
Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder
Suzanna G M Frints, Aysegul Ozanturk, Germán Rodríguez Criado, et al.
Neuro-Oncology
|
June 11, 2021
Characteristics of patients ≥10 years of age with diffuse intrinsic pontine glioma: a report from the International DIPG/DMG Registry
Craig Erker, Adam Lane, Brooklyn Chaney, et al.
Human Molecular Genetics
|
March 12, 2016
A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20
Neil A Hanchard, Shanker Swaminathan, Kristine Bucasas, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 12, 2023
Anomalies in the review process and interpretation of the evidence in the NICE guideline for chronic fatigue syndrome and myalgic encephalomyelitis
Peter White, Susan Abbey, Brian Angus, et al.
Genome Biology
|
March 27, 2014
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge
Catherine A Brownstein, Alan H Beggs, Nils Homer, et al.
Page
of 30
Search research articles
Search
Showing results (281-290 of 291) with videos related to
Sort By:
Page
of 30
HGG Advances
|
September 4, 2023
Rare variants in <i>CAPN2</i> increase risk for isolated hypoplastic left heart syndrome
Elizabeth E Blue, Janson J White, Michael K Dush, et al.
Viruses
|
June 11, 2020
Tenth Scientific Biennial Meeting of the Australasian Virology Society-AVS10 2019
Karla J Helbig, Rowena A Bull, Rebecca Ambrose, et al.
Acta Neuropathologica Communications
|
April 8, 2021
Molecular classification of a complex structural rearrangement of the RB1 locus in an infant with sporadic, isolated, intracranial, sellar region retinoblastoma
Kathleen M Schieffer, Alexander Z Feldman, Esko A Kautto, et al.
BMC Genomics
|
December 5, 2021
Discovery of clinically relevant fusions in pediatric cancer
Stephanie LaHaye, James R Fitch, Kyle J Voytovich, et al.
HGG Advances
|
December 10, 2021
Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease
Polakit Teekakirikul, Wenjuan Zhu, George C Gabriel, et al.
Molecular Psychiatry
|
May 6, 2018
Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder
Suzanna G M Frints, Aysegul Ozanturk, Germán Rodríguez Criado, et al.
Neuro-Oncology
|
June 11, 2021
Characteristics of patients ≥10 years of age with diffuse intrinsic pontine glioma: a report from the International DIPG/DMG Registry
Craig Erker, Adam Lane, Brooklyn Chaney, et al.
Human Molecular Genetics
|
March 12, 2016
A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20
Neil A Hanchard, Shanker Swaminathan, Kristine Bucasas, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 12, 2023
Anomalies in the review process and interpretation of the evidence in the NICE guideline for chronic fatigue syndrome and myalgic encephalomyelitis
Peter White, Susan Abbey, Brian Angus, et al.
Genome Biology
|
March 27, 2014
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge
Catherine A Brownstein, Alan H Beggs, Nils Homer, et al.
Page
of 30