Suchergebnisse - (Person:"Loundon, N")

PubPharm (5)

1

SOX10 mutations mimic isolated hearing loss

enthalten in: Clinical genetics | 2015

von Pingault, V. | Faubert, E. | Baral, V. | +9

2

Biallelic nonsense mutations in the otogelin-like gene (OTOGL) in a child affected by mild to moderate hearing impairment

enthalten in: Gene | 2013

von Bonnet, C. | Louha, M. | Loundon, N. | +12

3

Results of cochlear implantation in two children with mutations in the OTOF gene

enthalten in: International journal of pediatric otorhinolaryngology | 2006

von Rouillon, I. | Marcolla, A. | Roux, I. | +8

4

Auditory neuropathy or endocochlear hearing loss?

enthalten in: Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology | 2005

von Loundon, N. | Marcolla, A. | Roux, I. | +5

5

Screening of SLC26A4 (PDS) gene in Pendred's syndrome : a large spectrum of mutations in France and phenotypic heterogeneity

enthalten in: Clinical genetics | 2004

von Blons, H. | Feldmann, D. | Duval, V. | +20

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