Uncovering the roles of rare variants in common disease through whole-genome sequencing (Q37755970)

22 August 2017

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title

Uncovering the roles of rare variants in common disease through whole-genome sequencing (English)

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22 August 2017

whole genome sequencing

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1

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22 August 2017

David B Goldstein

2

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22 August 2017

1 June 2010

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22 August 2017

Nature Reviews Genetics

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22 August 2017

11

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22 August 2017

415-425

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22 August 2017

6

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https://scigraph.springernature.com/pub.10.1038/nrg2779

22 August 2017

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PubMed

https://pubmed.ncbi.nlm.nih.gov/20479773

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20479773

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Common disorders are quantitative traits

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20479773

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NRG2779

1 reference

22 August 2017

1 reference

PubMed ID

20479773