(Q50488717)

English

Hearing loss is a common feature of symptomatic children with profound biotinidase deficiency.

scientific article published in February 2002

In more languages

edit

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11865279

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/11865279

title

Hearing loss is a common feature of symptomatic children with profound biotinidase deficiency. (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11865279

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/11865279

1 reference

Barry Wolf

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11865279

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/11865279

Robert Spencer

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11865279

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/11865279

Tucker Gleason

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11865279

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/11865279

language of work or name

English

0 references

publication date

1 February 2002

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11865279

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/11865279

published in

The Journal of Pediatrics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11865279

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/11865279

volume

140

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11865279

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/11865279

issue

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11865279

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/11865279

page(s)

242-246

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11865279

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/11865279

Identifiers

DOI

10.1067/MPD.2002.121938

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11865279

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/11865279

PubMed publication ID

11865279

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11865279

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/11865279

(Q50488717)

Hearing loss is a common feature of symptomatic children with profound biotinidase deficiency.

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)