(Q34182809)

31 July 2017

title

Parents' interest in whole-genome sequencing of newborns (English)

1 reference

31 July 2017

main subject

whole genome sequencing

1 reference

Aaron J Goldenberg

1

1 reference

31 July 2017

Daniel S Dodson

series ordinal

2

1 reference

31 July 2017

Matthew M Davis

series ordinal

3

1 reference

31 July 2017

Beth A Tarini

series ordinal

4

1 reference

31 July 2017

language of work or name

English

0 references

publication date

6 June 2013

1 reference

31 July 2017

1 reference

31 July 2017

volume

16

1 reference

31 July 2017

issue

1

1 reference

31 July 2017

page(s)

78-84

1 reference

Technical report: Ethical and policy issues in genetic testing and screening of children

31 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164384

Sequencing from dried blood spots in infants with "false positive" newborn screen for MCAD deficiency

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164384

Applying Genomic Analysis to Newborn Screening

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164384

The ethical hazards and programmatic challenges of genomic newborn screening

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164384

Storage and use of residual newborn screening blood spots: a public policy emergency

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164384

Use of tandem mass spectrometry for multianalyte screening of dried blood specimens from newborns

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164384

Population-based newborn screening for genetic disorders when multiple mutation DNA testing is incorporated: a cystic fibrosis newborn screening model demonstrating increased sensitivity but more carrier detections

5 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FGIM.2013.76

Currents in contemporary ethics. State run newborn screening in the genomic era, or how to avoid drowning when drinking from a fire hose

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FGIM.2013.76

Currents in contemporary bioethics

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164384

Committee report: Considerations and recommendations for national guidance regarding the retention and use of residual dried blood spot specimens after newborn screening

28 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23743552

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Parents' interest in predictive genetic testing for their children when a disease has no treatment

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23743552

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Not without my permission: parents' willingness to permit use of newborn screening samples for research

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23743552

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/GIM.2013.76

1 reference

Dimensions Publication ID

31 July 2017

0 references

1 reference

31 July 2017

1 reference