(Q79224050)

English

A novel familial germline mutation in the initiator codon of the BHD gene in a patient with Birt-Hogg-Dubé syndrome

scientific article published on 01 November 2006

In more languages

edit

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed ID

17034545

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17034545%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 December 2019

title

A novel familial germline mutation in the initiator codon of the BHD gene in a patient with Birt-Hogg-Dubé syndrome (English)

1 reference

stated in

Europe PubMed Central

PubMed ID

17034545

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17034545%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

3

1 reference

stated in

Europe PubMed Central

PubMed ID

17034545

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17034545%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 December 2019

author name string

Bessis D

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed ID

17034545

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17034545%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 December 2019

Giraud S

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed ID

17034545

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17034545%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 December 2019

language of work or name

English

0 references

publication date

1 November 2006

1 reference

stated in

Europe PubMed Central

PubMed ID

17034545

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17034545%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 December 2019

published in

British Journal of Dermatology

1 reference

stated in

Europe PubMed Central

PubMed ID

17034545

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17034545%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 December 2019

volume

155

1 reference

stated in

Europe PubMed Central

PubMed ID

17034545

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17034545%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 December 2019

page(s)

1067-1069

1 reference

stated in

Europe PubMed Central

PubMed ID

17034545

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17034545%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 December 2019

issue

5

1 reference

stated in

Europe PubMed Central

PubMed ID

17034545

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17034545%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 December 2019

Identifiers

DOI

10.1111/J.1365-2133.2006.07449.X

1 reference

stated in

Europe PubMed Central

PubMed ID

17034545

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17034545%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

1 reference

Europe PubMed Central

PubMed ID

17034545

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17034545%20AND%20SRC:MED&resulttype=core&format=json

(Q79224050)

A novel familial germline mutation in the initiator codon of the BHD gene in a patient with Birt-Hogg-Dubé syndrome

Statements

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)