Confirmatory Results
A meta-analysis of the diagnostic sensitivity and clinical utility of genome sequencing, exome sequencing and chromosomal microarray in children with suspected genetic diseases
Michelle M. Clark, Zornitza Stark, Lauge Farnaes, Tiong Y. Tan, Susan M. White, David Dimmock, Stephen F. Kingsmore
doi: https://doi.org/10.1101/255299
Michelle M. Clark
1Rady Children’s Institute for Genomic Medicine, San Diego, CA, USA
PhDZornitza Stark
2Murdoch Children’s Research Institute, Melbourne, Australia
DMLauge Farnaes
1Rady Children’s Institute for Genomic Medicine, San Diego, CA, USA
3Department of Pediatrics, University of California San Diego, San Diego, CA, USA
MD PhDTiong Y. Tan
2Murdoch Children’s Research Institute, Melbourne, Australia
4Department of Paediatrics, University of Melbourne, Melbourne, Australia.
MD PhDSusan M. White
2Murdoch Children’s Research Institute, Melbourne, Australia
4Department of Paediatrics, University of Melbourne, Melbourne, Australia.
MDDavid Dimmock
1Rady Children’s Institute for Genomic Medicine, San Diego, CA, USA
MDStephen F. Kingsmore
1Rady Children’s Institute for Genomic Medicine, San Diego, CA, USA
MB ChB BAO DSc
Posted January 30, 2018.
A meta-analysis of the diagnostic sensitivity and clinical utility of genome sequencing, exome sequencing and chromosomal microarray in children with suspected genetic diseases
Michelle M. Clark, Zornitza Stark, Lauge Farnaes, Tiong Y. Tan, Susan M. White, David Dimmock, Stephen F. Kingsmore
bioRxiv 255299; doi: https://doi.org/10.1101/255299
A meta-analysis of the diagnostic sensitivity and clinical utility of genome sequencing, exome sequencing and chromosomal microarray in children with suspected genetic diseases
Michelle M. Clark, Zornitza Stark, Lauge Farnaes, Tiong Y. Tan, Susan M. White, David Dimmock, Stephen F. Kingsmore
bioRxiv 255299; doi: https://doi.org/10.1101/255299
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