Variation among Consent Forms for Clinical Whole Exome Sequencing

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1573-3599

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Variation among Consent Forms for Clinical Whole Exome Sequencing ; day:8 ; month:7 ; year:2017 ; pages:1-11
Journal of genetic counseling ; (8.7.2017), 1-11

Keyword: Diagnose
Diagnostik
Differentialdiagnose
Pflegediagnose

Creator: Fowler, Sara A.

Contributor: Saunders, Carol J.
Hoffman, Mark A.
SpringerLink (Online service)

DOI: 10.1007/s10897-017-0127-2

URN: urn:nbn:de:1111-201708165909

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:26 AM CEST

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Fowler, Sara A.
Saunders, Carol J.
Hoffman, Mark A.
SpringerLink (Online service)

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Screening the human exome: a comparison of whole genome and whole transcriptome sequencing

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Variation among Consent Forms for Clinical Whole Exome Sequencing

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Other Objects (12)

Readability of informed consent forms for whole-exome and whole-genome sequencing

Whole exome sequencing in the rat

Comparative study of whole exome sequencing-based copy number variation detection tools

Mutation discovery in mice by whole exome sequencing

Whole-exome sequencing of a pedigree segregating asthma

Opportunities and challenges of whole-genome and -exome sequencing

Enhanced whole exome sequencing by higher DNA insert lengths

Whole exome sequencing analysis identifies genes for alcohol consumption

An evaluation of copy number variation detection tools for cancer using whole exome sequencing data

Analytical validation of whole exome and whole genome sequencing for clinical applications

Screening the human exome: a comparison of whole genome and whole transcriptome sequencing

Identification of breast cancer susceptibility genes using whole exome sequencing

Readability of informed consent forms for whole-exome and whole-genome sequencing

Whole exome sequencing in the rat

Comparative study of whole exome sequencing-based copy number variation detection tools

Mutation discovery in mice by whole exome sequencing

Whole-exome sequencing of a pedigree segregating asthma

Opportunities and challenges of whole-genome and -exome sequencing

Enhanced whole exome sequencing by higher DNA insert lengths

Whole exome sequencing analysis identifies genes for alcohol consumption

An evaluation of copy number variation detection tools for cancer using whole exome sequencing data

Analytical validation of whole exome and whole genome sequencing for clinical applications

Screening the human exome: a comparison of whole genome and whole transcriptome sequencing

Identification of breast cancer susceptibility genes using whole exome sequencing

Readability of informed consent forms for whole-exome and whole-genome sequencing

Whole exome sequencing in the rat

Comparative study of whole exome sequencing-based copy number variation detection tools

Mutation discovery in mice by whole exome sequencing

Whole-exome sequencing of a pedigree segregating asthma

Opportunities and challenges of whole-genome and -exome sequencing

Enhanced whole exome sequencing by higher DNA insert lengths

Whole exome sequencing analysis identifies genes for alcohol consumption

An evaluation of copy number variation detection tools for cancer using whole exome sequencing data

Analytical validation of whole exome and whole genome sequencing for clinical applications

Screening the human exome: a comparison of whole genome and whole transcriptome sequencing

Identification of breast cancer susceptibility genes using whole exome sequencing

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