(Q35907727)

11 August 2017

It's complicated: criteria for policy decisions for the clinical integration of genome-scale sequencing for reproductive decision making (English)

1 reference

11 August 2017

1 reference

1

Benjamin S Wilfond

1 reference

11 August 2017

Katrina Ab Goddard

2

1 reference

11 August 2017

1 July 2015

1 reference

Molecular genetics & genomic medicine

11 August 2017

1 reference

11 August 2017

3

1 reference

11 August 2017

4

1 reference

11 August 2017

239-242

1 reference

Newborn screening: the genomic challenge

11 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4521960

Population-based carrier screening for cystic fibrosis: a systematic review of 23 years of research.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4521960

ACMG position statement on prenatal/preconception expanded carrier screening

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4521960

An empirical estimate of carrier frequencies for 400+ causal Mendelian variants: results from an ethnically diverse clinical sample of 23,453 individuals

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4521960

Exome sequencing can improve diagnosis and alter patient management

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4521960

Clinical application of exome sequencing in undiagnosed genetic conditions

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4521960

Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4521960

Ethical considerations in choosing a model for population‐based cystic fibrosis carrier screening

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4521960

Genotype-phenotype relationships in cystic fibrosis

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4521960

Screening for cystic fibrosis carrier state

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4521960

Cystic fibrosis screening using the College panel: platform comparison and lessons learned from the first 20,000 samples.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4521960

Laboratory standards and guidelines for population-based cystic fibrosis carrier screening

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4521960

National policy development for the clinical application of genetic diagnostic technologies. Lessons from cystic fibrosis

24 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26247041

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Diagnostic clinical genome and exome sequencing

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26247041

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/MGG3.130

1 reference

11 August 2017

1 reference

PMC publication ID

4521960

11 August 2017

PubMed publication ID

26247041

1 reference

PMC publication ID

4521960