Results
|
1.
|
|
|
2.
|
|
|
3.
|
|
|
4.
|
|
|
5.
|
|
|
6.
|
|
|
7.
|
|
|
8.
|
|
|
9.
|
|
|
10.
|
|
|
11.
|
|
|
12.
|
|
|
13.
|
|
|
14.
|
Unilateral Sensorineural Hearing Loss: Medical Context and Etiology. [electronic resource] by
- Paul, Antoine
- Marlin, Sandrine
- Parodi, Marine
- Rouillon, Isabelle
- Guerlain, Joanne
- Pingault, Véronique
- Couloigner, Vincent
- Garabedian, Erea Noel
- Denoyelle, Françoise
- Loundon, Natalie
Producer: 20180807
In:
Audiology & neuro-otology vol. 22
Availability: No items available.
|
|
15.
|
|
|
16.
|
Temperature-sensitive auditory neuropathy associated with an otoferlin mutation: Deafening fever! [electronic resource] by
- Marlin, Sandrine
- Feldmann, Delphine
- Nguyen, Yann
- Rouillon, Isabelle
- Loundon, Natalie
- Jonard, Laurence
- Bonnet, Crystel
- Couderc, Remy
- Garabedian, Eréa Noel
- Petit, Christine
- Denoyelle, Françoise
Producer: 20100504
In:
Biochemical and biophysical research communications vol. 394
Availability: No items available.
|
|
17.
|
The GJB2 mutation R75Q can cause nonsyndromic hearing loss DFNA3 or hereditary palmoplantar keratoderma with deafness. [electronic resource] by
- Feldmann, Delphine
- Denoyelle, Françoise
- Blons, Hélène
- Lyonnet, Stanislas
- Loundon, Natalie
- Rouillon, Isabelle
- Hadj-Rabia, Smail
- Petit, Christine
- Couderc, Rémy
- Garabédian, Eréa-Noel
- Marlin, Sandrine
Producer: 20051017
In:
American journal of medical genetics. Part A vol. 137
Availability: No items available.
|
|
18.
|
Congenital cytomegalovirus is the second most frequent cause of bilateral hearing loss in young French children. [electronic resource] by
- Avettand-Fenoël, Véronique
- Marlin, Sandrine
- Vauloup-Fellous, Christelle
- Loundon, Natalie
- François, Martine
- Couloigner, Vincent
- Rouillon, Isabelle
- Drouin-Garraud, Valérie
- Laccourreye, Laurence
- Denoyelle, Françoise
- Guilleminot, Tiffany
- Grabar, Sophie
- Leruez-Ville, Marianne
Producer: 20130426
In:
The Journal of pediatrics vol. 162
Availability: No items available.
|
|
19.
|
Mutation m.3395A > G in MT-ND1 leads to variable pathologic manifestations. [electronic resource] by
- Gutiérrez Cortés, Nicolás
- Pertuiset, Claire
- Dumon, Elodie
- Börlin, Marine
- Da Costa, Barbara
- Le Guédard, Marina
- Stojkovic, Tanya
- Loundon, Natalie
- Rouillon, Isabelle
- Nadjar, Yann
- Letellier, Thierry
- Jonard, Laurence
- Marlin, Sandrine
- Rocher, Christophe
Producer: 20210705
In:
Human molecular genetics vol. 29
Availability: No items available.
|
|
20.
|
High prevalence of congenital deafness on Reunion Island is due to a founder variant of LHFPL5. [electronic resource] by
- Lerat, Justine
- Bonnet, Crystel
- Cartault, François
- Loundon, Natalie
- Jacquemont, Marie-Line
- Darcel, Françoise
- Rouillon, Isabelle
- Mezouaghi, Kheira
- Guichet, Agnes
- Litzler, Julie
- Gesny, Roselyne
- Gherbi, Souad
- Aissa, Ines Ben
- Digeon, Fabienne Saint James
- Garabedian, Eréa-Nöel
- Bonnefont, Jean-Paul
- Genin, Emmanuelle
- Denoyelle, Françoise
- Jonard, Laurence
- Marlin, Sandrine
Producer: 20200211
In:
Clinical genetics vol. 95
Availability: No items available.
|