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BMC Genomics
|
August 23, 2012
Genomic variation in the vomeronasal receptor gene repertoires of inbred mice
Elizabeth H Wynn, Gabriela Sánchez-Andrade, Keren J Carss, et al.
Journal of Clinical Medicine
|
August 4, 2015
Exome Sequencing in Fetuses with Structural Malformations
Fiona L Mackie, Keren J Carss, Sarah C Hillman, et al.
Human Molecular Genetics
|
January 31, 2014
Exome sequencing improves genetic diagnosis of structural fetal abnormalities revealed by ultrasound
Keren J Carss, Sarah C Hillman, Vijaya Parthiban, et al.
Ophthalmic Genetics
|
November 20, 2018
Whole genome sequencing reveals novel mutations causing autosomal dominant inherited macular degeneration
Shyamanga Borooah, Chloe M Stanton, Joseph Marsh, et al.
Frontiers in Genetics
|
July 19, 2019
Rare Genetic Variation in 135 Families With Family History Suggestive of X-Linked Intellectual Disability
Alba Sanchis-Juan, Christina Bitsara, Kay Yi Low, et al.
Molecular Genetics & Genomic Medicine
|
April 30, 2020
Structural analysis of pathogenic missense mutations in GABRA2 and identification of a novel de novo variant in the desensitization gate
Alba Sanchis-Juan, Marcia A Hasenahuer, James A Baker, et al.
JAMA Cardiology
|
December 16, 2020
Assessing the Role of Rare Genetic Variation in Patients With Heart Failure
Gundula Povysil, Olympe Chazara, Keren J Carss, et al.
Molecular Vision
|
September 14, 2018
Novel homozygous splicing mutations in
Alessia Fiorentino, Jing Yu, Gavin Arno, et al.
Nature Reviews. Drug Discovery
|
October 19, 2022
Using human genetics to improve safety assessment of therapeutics
Keren J Carss, Aimee M Deaton, Alberto Del Rio-Espinola, et al.
Retina (Philadelphia, Pa.)
|
February 25, 2017
DETAILED RETINAL IMAGING IN CARRIERS OF OCULAR ALBINISM
Kamron N Khan, Emma C Lord, Gavin Arno, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 35) with videos related to
Sort By:
Page
of 4
BMC Genomics
|
August 23, 2012
Genomic variation in the vomeronasal receptor gene repertoires of inbred mice
Elizabeth H Wynn, Gabriela Sánchez-Andrade, Keren J Carss, et al.
Journal of Clinical Medicine
|
August 4, 2015
Exome Sequencing in Fetuses with Structural Malformations
Fiona L Mackie, Keren J Carss, Sarah C Hillman, et al.
Human Molecular Genetics
|
January 31, 2014
Exome sequencing improves genetic diagnosis of structural fetal abnormalities revealed by ultrasound
Keren J Carss, Sarah C Hillman, Vijaya Parthiban, et al.
Ophthalmic Genetics
|
November 20, 2018
Whole genome sequencing reveals novel mutations causing autosomal dominant inherited macular degeneration
Shyamanga Borooah, Chloe M Stanton, Joseph Marsh, et al.
Frontiers in Genetics
|
July 19, 2019
Rare Genetic Variation in 135 Families With Family History Suggestive of X-Linked Intellectual Disability
Alba Sanchis-Juan, Christina Bitsara, Kay Yi Low, et al.
Molecular Genetics & Genomic Medicine
|
April 30, 2020
Structural analysis of pathogenic missense mutations in GABRA2 and identification of a novel de novo variant in the desensitization gate
Alba Sanchis-Juan, Marcia A Hasenahuer, James A Baker, et al.
JAMA Cardiology
|
December 16, 2020
Assessing the Role of Rare Genetic Variation in Patients With Heart Failure
Gundula Povysil, Olympe Chazara, Keren J Carss, et al.
Molecular Vision
|
September 14, 2018
Novel homozygous splicing mutations in
Alessia Fiorentino, Jing Yu, Gavin Arno, et al.
Nature Reviews. Drug Discovery
|
October 19, 2022
Using human genetics to improve safety assessment of therapeutics
Keren J Carss, Aimee M Deaton, Alberto Del Rio-Espinola, et al.
Retina (Philadelphia, Pa.)
|
February 25, 2017
DETAILED RETINAL IMAGING IN CARRIERS OF OCULAR ALBINISM
Kamron N Khan, Emma C Lord, Gavin Arno, et al.
Page
of 4