(Q45736566)

15 December 2017

title

Targeted next-generation sequencing can replace Sanger sequencing in clinical diagnostics (English)

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15 December 2017

9

Rolf H Sijmons

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15 December 2017

author name string

Birgit Sikkema-Raddatz

1

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15 December 2017

Lennart F Johansson

2

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15 December 2017

Eddy N de Boer

3

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15 December 2017

Rowida Almomani

4

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15 December 2017

Ludolf G Boven

5

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15 December 2017

Maarten P van den Berg

6

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15 December 2017

Karin Y van Spaendonck-Zwarts

7

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15 December 2017

J Peter van Tintelen

8

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15 December 2017

Jan D H Jongbloed

10

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15 December 2017

Richard J Sinke

11

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15 December 2017

publication date

29 April 2013

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15 December 2017

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15 December 2017

volume

34

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15 December 2017

issue

7

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15 December 2017

page(s)

1035-1042

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Diagnostic exome sequencing in persons with severe intellectual disability

15 December 2017

cites work

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https://api.crossref.org/works/10.1002%2FHUMU.22332

Assuring the quality of next-generation sequencing in clinical laboratory practice

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https://api.crossref.org/works/10.1002%2FHUMU.22332

Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22332

Disease gene identification strategies for exome sequencing

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22332

Evaluation of second-generation sequencing of 19 dilated cardiomyopathy genes for clinical applications

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22332

De novo mutations of SETBP1 cause Schinzel-Giedion syndrome

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22332

New clinical molecular diagnostic methods for congenital and inherited heart disease

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22332

Exome sequencing identifies the cause of a mendelian disorder

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22332

Targeted capture and massively parallel sequencing of 12 human exomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22332

Next-generation sequencing to identify genetic causes of cardiomyopathies

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22332

A de novo paradigm for mental retardation.

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22332

Truncations of titin causing dilated cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22332

Comparison of solution-based exome capture methods for next generation sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22332

Assessment of target enrichment platforms using massively parallel sequencing for the mutation detection for congenital muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22332

Next generation sequencing for clinical diagnostics-principles and application to targeted resequencing for hypertrophic cardiomyopathy: a paper from the 2009 William Beaumont Hospital Symposium on Molecular Pathology

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22332

Application of next generation sequencing to molecular diagnosis of inherited diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22332

Erratum: Corrigendum: Performance comparison of benchtop high-throughput sequencing platforms

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22332

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1002/HUMU.22332

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15 December 2017

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