Comparison of the clinical manifestations of cystic fibrosis in black and white patients (Q34460732)

2 August 2017

Comparison of the clinical manifestations of cystic fibrosis in black and white patients (English)

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2 August 2017

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Hamosh A

1

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2 August 2017

FitzSimmons SC

2

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2 August 2017

Macek M Jr

3

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2 August 2017

Knowles MR

4

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2 August 2017

Rosenstein BJ

5

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2 August 2017

Cutting GR

6

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2 August 2017

language of work or name

English

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publication date

1 February 1998

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The Journal of Pediatrics

2 August 2017

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2 August 2017

132

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2 August 2017

2

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2 August 2017

255-259

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Cystic fibrosis in blacks in Washington, DC: incidence and characteristics

2 August 2017

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https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970441-X

Population variation of common cystic fibrosis mutations. The Cystic Fibrosis Genetic Analysis Consortium

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970441-X

A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970441-X

Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970441-X

Course of cystic fibrosis in black patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970441-X

The changing epidemiology of cystic fibrosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970441-X

Ventilatory functions of normal children and young adults—Mexican-American, white, and black. I. Spirometry

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970441-X

Efficacy of statewide neonatal screening for cystic fibrosis by assay of trypsinogen concentrations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970441-X

Sensitivity of the denaturing gradient gel electrophoresis technique in detection of known mutations and novel Asian mutations in the CFTR gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970441-X

Modulation of disease severity in cystic fibrosis transmembrane conductance regulator deficient mice by a secondary genetic factor

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970441-X

The relation between genotype and phenotype in cystic fibrosis--analysis of the most common mutation (delta F508).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970441-X

10.1016/S0022-3476(98)70441-X

7 January 2021

Identifiers

DOI

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2 August 2017

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