(Q48131962)

8 February 2018

title

Universal newborn hearing screening: a 27-month experience in the French region of Champagne-Ardenne. (English)

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8 February 2018

author name string

Marianne Lévêque

1

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8 February 2018

Pascal Schmidt

2

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Bernard Leroux

3

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Jean-Baptiste Danvin

4

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Thibault Langagne

5

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Marc Labrousse

6

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André Chays

7

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language of work or name

English

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publication date

18 June 2007

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8 February 2018

published in

Acta Paediatrica

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volume

96

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page(s)

1150-1154

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issue

8

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[Hereditary deafness: molecular genetics].

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21 January 2018

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Success rate of newborn and follow-up screening of hearing using otoacoustic emissions.

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The Colorado newborn hearing screening project, 1992-1999: on the threshold of effective population-based universal newborn hearing screening

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Combined microtia and aural atresia: issues in cochlear implantation

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Neonatal screening for hearing impairment--The Oman experience.

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Q829X, a novel mutation in the gene encoding otoferlin (OTOF), is frequently found in Spanish patients with prelingual non-syndromic hearing loss.

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The economic costs of congenital bilateral permanent childhood hearing impairment.

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Identifiers

DOI

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8 February 2018

PubMed ID

17578491

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8 February 2018