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American Journal of Human Genetics
|
March 5, 2013
Constitutional mutations in RTEL1 cause severe dyskeratosis congenita
Amanda J Walne, Tom Vulliamy, Michael Kirwan, et al.
Genetics
|
November 22, 2005
Relative influences of crossing over and gene conversion on the pattern of linkage disequilibrium in Arabidopsis thaliana
Vincent Plagnol, Badri Padhukasahasram, Jeffrey D Wall, et al.
Plos Genetics
|
May 22, 2007
A method to address differential bias in genotyping in large-scale association studies
Vincent Plagnol, Jason D Cooper, John A Todd, et al.
Archives of Oral Biology
|
April 16, 2015
A novel frameshift MSX1 mutation in a Saudi family with autosomal dominant premolar and third molar agenesis
Shurog AlFawaz, Vincent Plagnol, Ferranti S L Wong, et al.
Biostatistics (Oxford, England)
|
November 29, 2008
Statistical independence of the colocalized association signals for type 1 diabetes and RPS26 gene expression on chromosome 12q13
Vincent Plagnol, Deborah J Smyth, John A Todd, et al.
BMC Medical Genomics
|
May 28, 2017
Quantitative analysis of cryptic splicing associated with TDP-43 depletion
Jack Humphrey, Warren Emmett, Pietro Fratta, et al.
Journal of Medical Genetics
|
October 12, 2012
Use of targeted exome sequencing as a diagnostic tool for Familial Hypercholesterolaemia
Marta Futema, Vincent Plagnol, Ros A Whittall, et al.
Neuroscience Letters
|
May 8, 2012
Study of the genetic variability in a Parkinson's Disease gene: EIF4G1
Arianna Tucci, Gavin Charlesworth, Una-Marie Sheerin, et al.
Plos One
|
August 14, 2008
Extreme clonality in lymphoblastoid cell lines with implications for allele specific expression analyses
Vincent Plagnol, Elif Uz, Chris Wallace, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
December 7, 2007
Interactions between Idd5.1/Ctla4 and other type 1 diabetes genes
Kara Hunter, Dan Rainbow, Vincent Plagnol, et al.
Page
of 19
Search research articles
Search
Showing results (11-20 of 189) with videos related to
Sort By:
Page
of 19
American Journal of Human Genetics
|
March 5, 2013
Constitutional mutations in RTEL1 cause severe dyskeratosis congenita
Amanda J Walne, Tom Vulliamy, Michael Kirwan, et al.
Genetics
|
November 22, 2005
Relative influences of crossing over and gene conversion on the pattern of linkage disequilibrium in Arabidopsis thaliana
Vincent Plagnol, Badri Padhukasahasram, Jeffrey D Wall, et al.
Plos Genetics
|
May 22, 2007
A method to address differential bias in genotyping in large-scale association studies
Vincent Plagnol, Jason D Cooper, John A Todd, et al.
Archives of Oral Biology
|
April 16, 2015
A novel frameshift MSX1 mutation in a Saudi family with autosomal dominant premolar and third molar agenesis
Shurog AlFawaz, Vincent Plagnol, Ferranti S L Wong, et al.
Biostatistics (Oxford, England)
|
November 29, 2008
Statistical independence of the colocalized association signals for type 1 diabetes and RPS26 gene expression on chromosome 12q13
Vincent Plagnol, Deborah J Smyth, John A Todd, et al.
BMC Medical Genomics
|
May 28, 2017
Quantitative analysis of cryptic splicing associated with TDP-43 depletion
Jack Humphrey, Warren Emmett, Pietro Fratta, et al.
Journal of Medical Genetics
|
October 12, 2012
Use of targeted exome sequencing as a diagnostic tool for Familial Hypercholesterolaemia
Marta Futema, Vincent Plagnol, Ros A Whittall, et al.
Neuroscience Letters
|
May 8, 2012
Study of the genetic variability in a Parkinson's Disease gene: EIF4G1
Arianna Tucci, Gavin Charlesworth, Una-Marie Sheerin, et al.
Plos One
|
August 14, 2008
Extreme clonality in lymphoblastoid cell lines with implications for allele specific expression analyses
Vincent Plagnol, Elif Uz, Chris Wallace, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
December 7, 2007
Interactions between Idd5.1/Ctla4 and other type 1 diabetes genes
Kara Hunter, Dan Rainbow, Vincent Plagnol, et al.
Page
of 19