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X-linked mixed deafness (DFN3): cloning and characterization of the critical region allows the identification of novel microdeletions. [electronic resource] by
- Huber, I
- Bitner-Glindzicz, M
- de Kok, Y J
- van der Maarel, S M
- Ishikawa-Brush, Y
- Monaco, A P
- Robinson, D
- Malcolm, S
- Pembrey, M E
- Brunner, H G
Producer: 19950105
In:
Human molecular genetics vol. 3
Availability: No items available.
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