(Q50506244)

English

Deafness due to Pro250Arg mutation of FGFR3.

scientific article published in March 1998

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9525367

Deafness due to Pro250Arg mutation of FGFR3. (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9525367

1 reference

based on heuristic

inferred from title

author name string

G E Hollway

1

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9525367

G K Suthers

2

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9525367

K M Battese

3

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9525367

A M Turner

4

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9525367

D J David

5

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9525367

J C Mulley

6

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9525367

language of work or name

0 references

publication date

1 March 1998

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9525367

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9525367

351

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9525367

9106

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9525367

877-878

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9525367

Fibroblast-growth-factor receptor mutations in human skeletal disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2898%2924012-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Prevalence of Pro250Arg mutation of fibroblast growth factor receptor 3 in coronal craniosynostosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2898%2924012-8

7 January 2021

based on heuristic

inferred from DOI database lookup

A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2898%2924012-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2898%2924012-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0140-6736(98)24012-8

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9525367

release_maphcdtxcvbwvmsgqxadcov6fi

1 reference

https://api.fatcat.wiki/v0/release/maphcdtxcvbwvmsgqxadcov6fi

24 November 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9525367

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)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q50506244&oldid=2117390272"