Results
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Results of cochlear implantation in two children with mutations in the OTOF gene. [electronic resource] by
- Rouillon, I
- Marcolla, A
- Roux, I
- Marlin, S
- Feldmann, D
- Couderc, R
- Jonard, L
- Petit, C
- Denoyelle, F
- Garabédian, E N
- Loundon, N
Producer: 20060922
In:
International journal of pediatric otorhinolaryngology vol. 70
Availability: No items available.
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130.
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Fourth case of cerebral, ocular, dental, auricular, skeletal syndrome (CODAS), description of new features and molecular analysis. [electronic resource] by
- Marlin, S
- Ducou Le Pointe, H
- Le Merrer, M
- Portnoi, M F
- Chantot, S
- Jonard, L
- Mantel-Guiochon, A
- Siffroi, J P
- Garabedian, E N
- Denoyelle, F
Producer: 20100830
In:
American journal of medical genetics. Part A vol. 152A
Availability: No items available.
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133.
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Biallelic nonsense mutations in the otogelin-like gene (OTOGL) in a child affected by mild to moderate hearing impairment. [electronic resource] by
- Bonnet, C
- Louha, M
- Loundon, N
- Michalski, N
- Verpy, E
- Smagghe, L
- Hardelin, J-P
- Rouillon, I
- Jonard, L
- Couderc, R
- Gherbi, S
- Garabedian, E N
- Denoyelle, F
- Petit, C
- Marlin, S
Producer: 20131030
In:
Gene vol. 527
Availability: No items available.
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134.
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Impaired prostate tumorigenesis in Egr1-deficient mice. [electronic resource] by
- Abdulkadir, S A
- Qu, Z
- Garabedian, E
- Song, S K
- Peters, T J
- Svaren, J
- Carbone, J M
- Naughton, C K
- Catalona, W J
- Ackerman, J J
- Gordon, J I
- Humphrey, P A
- Milbrandt, J
Producer: 20010222
In:
Nature medicine vol. 7
Availability: No items available.
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135.
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Screening of SLC26A4 (PDS) gene in Pendred's syndrome: a large spectrum of mutations in France and phenotypic heterogeneity. [electronic resource] by
- Blons, H
- Feldmann, D
- Duval, V
- Messaz, O
- Denoyelle, F
- Loundon, N
- Sergout-Allaoui, A
- Houang, M
- Duriez, F
- Lacombe, D
- Delobel, B
- Leman, J
- Catros, H
- Journel, H
- Drouin-Garraud, V
- Obstoy, M-F
- Toutain, A
- Oden, S
- Toublanc, J E
- Couderc, R
- Petit, C
- Garabédian, E-N
- Marlin, S
Producer: 20050208
In:
Clinical genetics vol. 66
Availability: No items available.
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136.
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Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene. [electronic resource] by
- Denoyelle, F
- Weil, D
- Maw, M A
- Wilcox, S A
- Lench, N J
- Allen-Powell, D R
- Osborn, A H
- Dahl, H H
- Middleton, A
- Houseman, M J
- Dodé, C
- Marlin, S
- Boulila-ElGaïed, A
- Grati, M
- Ayadi, H
- BenArab, S
- Bitoun, P
- Lina-Granade, G
- Godet, J
- Mustapha, M
- Loiselet, J
- El-Zir, E
- Aubois, A
- Joannard, A
- Levilliers, J
- Garabédian, E N
- Mueller, R F
- Gardner, R J
- Petit, C
Producer: 19971219
In:
Human molecular genetics vol. 6
Availability: No items available.
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