(Q73433869)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10668931%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

title

Polyvariant mutant CFTR genes in patients with chronic pancreatitis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10668931%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference

C Arduino

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10668931%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

M Gallo

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10668931%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

A Brusco

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10668931%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

S Garnerone

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10668931%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

M R Piana

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10668931%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

S Di Maggio

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10668931%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

G Gerbino Promis

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10668931%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

M Ferrone

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10668931%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

A Angeli

9

1 reference

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3 November 2019

E Gaia

10

1 reference

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3 November 2019

publication date

1 November 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10668931%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

number of pages

5

1 reference

inferred from page(s)

published in

Clinical Genetics

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10668931%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

volume

56

1 reference

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3 November 2019

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10668931%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

page(s)

400-404

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10668931%20AND%20SRC:MED&resulttype=core&format=json

Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene

3 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560509.X

7 January 2021

Mutations in the cationic trypsinogen gene are associated with recurrent acute and chronic pancreatitis

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560509.X

7 January 2021

Relation between mutations of the cystic fibrosis gene and idiopathic pancreatitis.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560509.X

7 January 2021

Mutations of the cystic fibrosis gene in patients with chronic pancreatitis

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560509.X

7 January 2021

Polyvariant mutant cystic fibrosis transmembrane conductance regulator genes. The polymorphic (Tg)m locus explains the partial penetrance of the T5 polymorphism as a disease mutation

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560509.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560509.X

7 January 2021

Restriction site generating-polymerase chain reaction (RG-PCR) for the probeless detection of hidden genetic variation: application to the study of some common cystic fibrosis mutations

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560509.X

7 January 2021

Sensitivity of single-strand conformation polymorphism and heteroduplex method for mutation detection in the cystic fibrosis gene.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560509.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560509.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560509.X

7 January 2021

Congenital bilateral absence of the vas deferens and cystic fibrosis. A genetic commonality.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560509.X

7 January 2021

Increased incidence of cystic fibrosis gene mutations in adults with disseminated bronchiectasis

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560509.X

7 January 2021

Pancreatitis and mutations of the cystic fibrosis gene

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560509.X

7 January 2021

A mutation in CFTR produces different phenotypes depending on chromosomal background

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560509.X

7 January 2021

Congenital bilateral absence of the vas deferens (CBAVD) and cystic fibrosis transmembrane regulator (CFTR): correlation between genotype and phenotype

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560509.X

7 January 2021

A Novel Mutation in the Cystic Fibrosis Gene in Patients with Pulmonary Disease but Normal Sweat Chloride Concentrations

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560509.X

7 January 2021

10.1034/J.1399-0004.1999.560509.X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10668931%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference