(Q34977704)

5 August 2017

Standards and guidelines for CFTR mutation testing (English)

1 reference

5 August 2017

Carolyn Sue Richards

1

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5 August 2017

Linda A Bradley

2

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5 August 2017

Jean Amos

3

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5 August 2017

Bernice Allitto

4

1 reference

5 August 2017

Wayne W Grody

5

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5 August 2017

Anne Maddalena

6

1 reference

5 August 2017

Matthew J McGinnis

7

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5 August 2017

Thomas W Prior

8

1 reference

5 August 2017

Bradley W Popovich

9

1 reference

5 August 2017

Michael S Watson

10

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5 August 2017

Glenn E Palomaki

11

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5 August 2017

language of work or name

English

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publication date

1 September 2002

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5 August 2017

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5 August 2017

4

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5 August 2017

379-391

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5 August 2017

5

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https://scigraph.springernature.com/pub.10.1097/00125817-200209000-00010

5 August 2017

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cites work

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

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00010

Identification of the cystic fibrosis gene: genetic analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00010

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00010

Identification of the cystic fibrosis gene: chromosome walking and jumping

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00010

A robotics-assisted procedure for large scale cystic fibrosis mutation analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00010

Detection of multiple cystic fibrosis mutations by reverse dot blot hybridization: a technology for carrier screening

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00010

Reverse dot blot probes for the screening of beta-thalassemia mutations in Asians and American blacks

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00010

A 31-mutation assay for cystic fibrosis testing in the clinical molecular diagnostics laboratory

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00010

A Multiplex ARMS Test for 10 Cystic Fibrosis (CF) Mutations: Evaluation in a Prenatal CF Screening Program

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00010

Development and validation of a screening test for 12 common mutations of the cystic fibrosis CFTR gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00010

Evaluation of laboratory methods for cystic fibrosis carrier screening: reliability, sensitivity, specificity, and costs

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00010

Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00010

Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00010

Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00010

Improved detection of cystic fibrosis mutations in the heterogeneous U.S. population using an expanded, pan-ethnic mutation panel

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00010

Calculating posterior cystic fibrosis risk with echogenic bowel and one characterized cystic fibrosis mutation: avoiding pitfalls in the risk calculations

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00010

10.1097/00125817-200209000-00010

21 January 2018

Identifiers

DOI

1 reference

Dimensions Publication ID

5 August 2017

0 references

1 reference