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Progressive hereditary hearing impairment caused by a MYO6 mutation resembles presbyacusis. [electronic resource] by
- Oonk, A M M
- Leijendeckers, J M
- Lammers, E M
- Weegerink, N J D
- Oostrik, J
- Beynon, A J
- Huygen, P L M
- Kunst, H P M
- Kremer, H
- Snik, A F M
- Pennings, R J E
Producer: 20131028
In:
Hearing research vol. 299
Availability: No items available.
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13.
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Further audiovestibular characterization of DFNB77, caused by deleterious variants in LOXHD1, and investigation into the involvement of Fuchs corneal dystrophy. [electronic resource] by
- Wesdorp, M
- Schreur, V
- Beynon, A J
- Oostrik, J
- van de Kamp, J M
- Elting, M W
- van den Boogaard, M-J H
- Feenstra, I
- Admiraal, R J C
- Kunst, H P M
- Hoyng, C B
- Kremer, H
- Yntema, H G
- Pennings, R J E
- Schraders, M
Producer: 20191115
In:
Clinical genetics vol. 94
Availability: No items available.
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