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Nature Communications
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June 27, 2017
Prevalence of sexual dimorphism in mammalian phenotypic traits
Natasha A Karp, Jeremy Mason, Arthur L Beaudet, et al.
Nature Communications
|
February 2, 2020
Human and mouse essentiality screens as a resource for disease gene discovery
Pilar Cacheiro, Violeta Muñoz-Fuentes, Stephen A Murray, et al.
Genome Biology
|
February 4, 2020
The Deep Genome Project
K C Kent Lloyd, David J Adams, Gareth Baynam, et al.
The New England Journal of Medicine
|
June 20, 2019
Reanalysis of Clinical Exome Sequencing Data
Pengfei Liu, Linyan Meng, Elizabeth A Normand, et al.
Nature Communications
|
October 14, 2017
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction
Michael R Bowl, Michelle M Simon, Neil J Ingham, et al.
Genome Medicine
|
September 23, 2017
Identification of novel candidate disease genes from de novo exonic copy number variants
Tomasz Gambin, Bo Yuan, Weimin Bi, et al.
Neuron
|
September 25, 2015
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci
Stephan J Sanders, Xin He, A Jeremy Willsey, et al.
JAMA Pediatrics
|
October 4, 2017
Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical Management
Linyan Meng, Mohan Pammi, Anirudh Saronwala, et al.
American Journal of Human Genetics
|
February 19, 2019
Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes
Lindsay C Burrage, John J Reynolds, Nissan Vida Baratang, et al.
Nature Genetics
|
June 27, 2017
Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium
Terrence F Meehan, Nathalie Conte, David B West, et al.
Page
of 19
Search research articles
Search
Showing results (171-180 of 190) with videos related to
Sort By:
Page
of 19
Nature Communications
|
June 27, 2017
Prevalence of sexual dimorphism in mammalian phenotypic traits
Natasha A Karp, Jeremy Mason, Arthur L Beaudet, et al.
Nature Communications
|
February 2, 2020
Human and mouse essentiality screens as a resource for disease gene discovery
Pilar Cacheiro, Violeta Muñoz-Fuentes, Stephen A Murray, et al.
Genome Biology
|
February 4, 2020
The Deep Genome Project
K C Kent Lloyd, David J Adams, Gareth Baynam, et al.
The New England Journal of Medicine
|
June 20, 2019
Reanalysis of Clinical Exome Sequencing Data
Pengfei Liu, Linyan Meng, Elizabeth A Normand, et al.
Nature Communications
|
October 14, 2017
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction
Michael R Bowl, Michelle M Simon, Neil J Ingham, et al.
Genome Medicine
|
September 23, 2017
Identification of novel candidate disease genes from de novo exonic copy number variants
Tomasz Gambin, Bo Yuan, Weimin Bi, et al.
Neuron
|
September 25, 2015
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci
Stephan J Sanders, Xin He, A Jeremy Willsey, et al.
JAMA Pediatrics
|
October 4, 2017
Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical Management
Linyan Meng, Mohan Pammi, Anirudh Saronwala, et al.
American Journal of Human Genetics
|
February 19, 2019
Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes
Lindsay C Burrage, John J Reynolds, Nissan Vida Baratang, et al.
Nature Genetics
|
June 27, 2017
Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium
Terrence F Meehan, Nathalie Conte, David B West, et al.
Page
of 19