(Q37689764)

22 August 2017

0 references

Clinical exome sequencing in daily practice: 1,000 patients and beyond (English)

1 reference

22 August 2017

Hans Scheffer

2

0 references

Joris A Veltman

object named as

Joris A Veltman

series ordinal

3

0 references

author name string

Wendy A van Zelst-Stams

series ordinal

1

1 reference

22 August 2017

24 January 2014

1 reference

22 August 2017

1 reference

22 August 2017

6

1 reference

22 August 2017

1

1 reference

22 August 2017

2

1 reference

https://scigraph.springernature.com/pub.10.1186/gm521

22 August 2017

0 references

cites work

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978472

Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978472

Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978472

Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978472

Performance comparison of exome DNA sequencing technologies

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978472

Targeted capture and massively parallel sequencing of 12 human exomes

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978472

Diagnostic exome sequencing in persons with severe intellectual disability

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978472

A de novo paradigm for mental retardation.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978472

A Post-Hoc Comparison of the Utility of Sanger Sequencing and Exome Sequencing for the Diagnosis of Heterogeneous Diseases

1 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2FGM521

21 January 2018

Identifiers

DOI

10.1186/GM521

1 reference

PMC publication ID

3978472

Dimensions Publication ID

22 August 2017

0 references

1 reference

PMC publication ID

3978472

22 August 2017

PubMed publication ID

24456652

1 reference

PMC publication ID

3978472