G59S mutation in the GJB2 (connexin 26) gene in a patient with Bart-Pumphrey syndrome (Q81842017)

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scientific article published on 01 July 2005

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English	G59S mutation in the GJB2 (connexin 26) gene in a patient with Bart-Pumphrey syndrome	scientific article published on 01 July 2005

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15952212

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15952212%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 January 2020

title

G59S mutation in the GJB2 (connexin 26) gene in a patient with Bart-Pumphrey syndrome (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15952212

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15952212%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 January 2020

main subject

Bart-Pumphrey syndrome

1 reference

based on heuristic

inferred from title

author

Antonia Paula Marques-de-Faria

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15952212

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15952212%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 January 2020

author name string

Fabiana Alexandrino

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15952212

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15952212%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 January 2020

Edi Lúcia Sartorato

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15952212

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15952212%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 January 2020

Carlos Eduardo Steiner

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15952212

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15952212%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 January 2020

publication date

1 July 2005

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15952212

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15952212%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 January 2020

published in

American Journal of Medical Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15952212

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15952212%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 January 2020

volume

136

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15952212

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15952212%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 January 2020

issue

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15952212

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15952212%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 January 2020

page(s)

282-284

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15952212

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15952212%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 January 2020

Identifiers

DOI

10.1002/AJMG.A.30822

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15952212

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15952212%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 January 2020

PubMed publication ID

15952212

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15952212

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15952212%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 January 2020

 

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