[HTML][HTML] A population genetic approach to mapping neurological disorder genes using deep resequencing
Deep resequencing of functional regions in human genomes is key to identifying potentially
causal rare variants for complex disorders. Here, we present the results from a large-sample …
causal rare variants for complex disorders. Here, we present the results from a large-sample …
A population genetic approach to mapping neurological disorder genes using deep resequencing
RA Myers, F Casals, J Gauthier, FF Hamdan… - PLoS …, 2011 - pubmed.ncbi.nlm.nih.gov
Deep resequencing of functional regions in human genomes is key to identifying potentially
causal rare variants for complex disorders. Here, we present the results from a large-sample …
causal rare variants for complex disorders. Here, we present the results from a large-sample …
[PDF][PDF] A Population Genetic Approach to Mapping Neurological Disorder Genes Using Deep
RA Myers, F Casals, J Gauthier, FF Hamdan, J Keebler - 2011 - pdfs.semanticscholar.org
Deep resequencing of functional regions in human genomes is key to identifying potentially
causal rare variants for complex disorders. Here, we present the results from a large-sample …
causal rare variants for complex disorders. Here, we present the results from a large-sample …
[PDF][PDF] A Population Genetic Approach to Mapping Neurological Disorder Genes Using Deep
RA Myers, F Casals, J Gauthier, FF Hamdan, J Keebler - 2011 - Citeseer
Deep resequencing of functional regions in human genomes is key to identifying potentially
causal rare variants for complex disorders. Here, we present the results from a large-sample …
causal rare variants for complex disorders. Here, we present the results from a large-sample …
A Population Genetic Approach to Mapping Neurological Disorder Genes Using Deep Resequencing
RA Myers, F Casals, J Gauthier, FF Hamdan… - PLoS …, 2011 - search.proquest.com
Deep resequencing of functional regions in human genomes is key to identifying potentially
causal rare variants for complex disorders. Here, we present the results from a large-sample …
causal rare variants for complex disorders. Here, we present the results from a large-sample …
[HTML][HTML] A Population Genetic Approach to Mapping Neurological Disorder Genes Using Deep Resequencing
RA Myers, F Casals, J Gauthier, FF Hamdan… - PLoS …, 2011 - ncbi.nlm.nih.gov
Deep resequencing of functional regions in human genomes is key to identifying potentially
causal rare variants for complex disorders. Here, we present the results from a large-sample …
causal rare variants for complex disorders. Here, we present the results from a large-sample …
A Population Genetic Approach to Mapping Neurological Disorder Genes Using Deep Resequencing
RA Myers, F Casals, J Gauthier, FF Hamdan… - PLOS …, 2011 - econpapers.repec.org
Deep resequencing of functional regions in human genomes is key to identifying potentially
causal rare variants for complex disorders. Here, we present the results from a large-sample …
causal rare variants for complex disorders. Here, we present the results from a large-sample …
A Population Genetic Approach to Mapping Neurological Disorder Genes Using Deep Resequencing
RA Myers, F Casals, J Gauthier, FF Hamdan, J Keebler… - 2011 - escholarship.mcgill.ca
Deep resequencing of functional regions in human genomes is key to identifying potentially
causal rare variants for complex disorders. Here, we present the results from a large-sample …
causal rare variants for complex disorders. Here, we present the results from a large-sample …
A population genetic approach to mapping neurological disorder genes using deep resequencing
RA Myers, F Casals, J Gauthier, FF Hamdan… - PLoS …, 2011 - go.gale.com
Deep resequencing of functional regions in human genomes is key to identifying potentially
causal rare variants for complex disorders. Here, we present the results from a large-sample …
causal rare variants for complex disorders. Here, we present the results from a large-sample …
A population genetic approach to mapping neurological disorder genes using deep resequencing.
RA Myers, F Casals, J Gauthier, FF Hamdan… - Plos Genetics, 2011 - europepmc.org
Deep resequencing of functional regions in human genomes is key to identifying potentially
causal rare variants for complex disorders. Here, we present the results from a large-sample …
causal rare variants for complex disorders. Here, we present the results from a large-sample …