Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
BJ O'Roak, P Deriziotis, C Lee, L Vives, JJ Schwartz… - Nature …, 2011 - nature.com
Evidence for the etiology of autism spectrum disorders (ASDs) has consistently pointed to a
strong genetic component complicated by substantial locus heterogeneity,. We sequenced …
strong genetic component complicated by substantial locus heterogeneity,. We sequenced …
[PDF][PDF] Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
JO Brian, P Deriziotis, C Lee, L Vives, JJ Schwartz… - Nat Genet, 2011 - researchgate.net
Evidence for the etiology of autism spectrum disorders (ASD) has consistently pointed to a
strong genetic component complicated by substantial locus heterogeneity1, 2. We …
strong genetic component complicated by substantial locus heterogeneity1, 2. We …
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
BJ O'Roak, P Deriziotis, C Lee, L Vives, JJ Schwartz… - Nature …, 2011 - pure.mpg.de
Evidence for the etiology of autism spectrum disorders (ASDs) has consistently pointed to a
strong genetic component complicated by substantial locus heterogeneity1, 2. We …
strong genetic component complicated by substantial locus heterogeneity1, 2. We …
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
BJ O'Roak, P Deriziotis, C Lee, L Vives, JJ Schwartz… - Nature …, 2011 - pure.psu.edu
Evidence for the etiology of autism spectrum disorders (ASDs) has consistently pointed to a
strong genetic component complicated by substantial locus heterogeneity. We sequenced …
strong genetic component complicated by substantial locus heterogeneity. We sequenced …
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
BJ O'Roak, P Deriziotis, C Lee, L Vives… - Nature …, 2011 - ohsu.elsevierpure.com
Evidence for the etiology of autism spectrum disorders (ASDs) has consistently pointed to a
strong genetic component complicated by substantial locus heterogeneity. We sequenced …
strong genetic component complicated by substantial locus heterogeneity. We sequenced …
[PDF][PDF] Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
JO Brian, P Deriziotis, C Lee, L Vives, JJ Schwartz… - Nat Genet, 2011 - rareconnect.org
Evidence for the etiology of autism spectrum disorders (ASD) has consistently pointed to a
strong genetic component complicated by substantial locus heterogeneity1, 2. We …
strong genetic component complicated by substantial locus heterogeneity1, 2. We …
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
BJ O'Roak, P Deriziotis, C Lee, L Vives… - Nature …, 2011 - pubmed.ncbi.nlm.nih.gov
Evidence for the etiology of autism spectrum disorders (ASDs) has consistently pointed to a
strong genetic component complicated by substantial locus heterogeneity. We sequenced …
strong genetic component complicated by substantial locus heterogeneity. We sequenced …
[HTML][HTML] Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
BJ O'Roak, P Deriziotis, C Lee, L Vives… - Nature …, 2011 - ncbi.nlm.nih.gov
Evidence for the etiology of autism spectrum disorders (ASD) has consistently pointed to a
strong genetic component complicated by substantial locus heterogeneity 1, 2. We …
strong genetic component complicated by substantial locus heterogeneity 1, 2. We …
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
BJ O'Roak, P Deriziotis, C Lee, L Vives… - Nature …, 2011 - search.ebscohost.com
Evidence for the etiology of autism spectrum disorders (ASDs) has consistently pointed to a
strong genetic component complicated by substantial locus heterogeneity. We sequenced …
strong genetic component complicated by substantial locus heterogeneity. We sequenced …
[引用][C] Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
BJ O'ROAK - Nat Genet, 2011 - cir.nii.ac.jp