De novo mutations revealed by whole-exome sequencing are strongly associated with autism
SJ Sanders, MT Murtha, AR Gupta, JD Murdoch…�- Nature, 2012 - nature.com
Multiple studies have confirmed the contribution of rare de novo copy number variations to
the risk for autism spectrum disorders,,. But whereas de novo single nucleotide variants�…
the risk for autism spectrum disorders,,. But whereas de novo single nucleotide variants�…
De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
SJ Sanders, MT Murtha, AR Gupta, JD Murdoch… - 2012 - psycnet.apa.org
Multiple studies have confirmed the contribution of rare de novo copy number variations to
the risk for autism spectrum disorders 1-3. But whereas de novo single nucleotide variants�…
the risk for autism spectrum disorders 1-3. But whereas de novo single nucleotide variants�…
[HTML][HTML] De novo mutations revealed by whole exome sequencing are strongly associated with autism
SJ Sanders, MT Murtha, AR Gupta, JD Murdoch…�- Nature - ncbi.nlm.nih.gov
Multiple studies have confirmed the contribution of rare de novo copy number variations
(CNVs) to the risk for Autism Spectrum Disorders (ASD). 1-3 While de novo single nucleotide�…
(CNVs) to the risk for Autism Spectrum Disorders (ASD). 1-3 While de novo single nucleotide�…
[PDF][PDF] De novo mutations revealed by whole-exome sequencing are strongly associated with autism
SJ Sanders, MT Murtha, AR Gupta, JD Murdoch… - 2012 - researchgate.net
Multiple studies have confirmed the contribution of rare de novo copy number variations to
the risk for autism spectrum disorders1–3. But whereas de novo single nucleotide variants�…
the risk for autism spectrum disorders1–3. But whereas de novo single nucleotide variants�…
De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
SJ Sanders, MT Murtha, AR Gupta, JD Murdoch…�- …, 2012 - search.ebscohost.com
Multiple studies have confirmed the contribution of rare de novo copy number variations to
the risk for autism spectrum disorders. But whereas de novo single nucleotide variants have�…
the risk for autism spectrum disorders. But whereas de novo single nucleotide variants have�…
De novo mutations revealed by whole-exome sequencing are strongly associated with autism
SJ Sanders, MT Murtha, AR Gupta, JD Murdoch…�- …, 2012 - ui.adsabs.harvard.edu
Multiple studies have confirmed the contribution of rare de novo copy number variations to
the risk for autism spectrum disorders. But whereas de novo single nucleotide variants have�…
the risk for autism spectrum disorders. But whereas de novo single nucleotide variants have�…
[CITATION][C] De novo mutations revealed by whole-exome sequencing are strongly associated with autism
SJ SANDERS, MT MURTHA, MF WALKER…�- Nature�…, 2012 - pascal-francis.inist.fr
De novo mutations revealed by whole-exome sequencing are strongly associated with
autism CNRS Inist Pascal-Francis CNRS Pascal and Francis Bibliographic Databases�…
autism CNRS Inist Pascal-Francis CNRS Pascal and Francis Bibliographic Databases�…
De novo mutations revealed by whole-exome sequencing are strongly associated with autism
SJ Sanders, MT Murtha, AR Gupta, JD Murdoch…�- Nature, 2012 - econpapers.repec.org
EconPapers: De novo mutations revealed by whole-exome sequencing are strongly associated
with autism EconPapers Economics at your fingertips EconPapers Home About EconPapers�…
with autism EconPapers Economics at your fingertips EconPapers Home About EconPapers�…
[CITATION][C] De novo mutations revealed by whole-exome sequencing are strongly associated with autism
SJ SANDERS�- Nature, 2012 - cir.nii.ac.jp
De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
SJ Sanders, MT Murtha, AR Gupta, JD Murdoch…�- Nature, 2012 - europepmc.org
Multiple studies have confirmed the contribution of rare de novo copy number variations
(CNVs) to the risk for Autism Spectrum Disorders (ASD). 1-3 While de novo single nucleotide�…
(CNVs) to the risk for Autism Spectrum Disorders (ASD). 1-3 While de novo single nucleotide�…