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506.
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Exclusion of mutations in the PRNP, JPH3, TBP, ATN1, CREBBP, POU3F2 and FTL genes as a cause of disease in Portuguese patients with a Huntington-like phenotype. [electronic resource] by
- Costa, Maria do Carmo
- Teixeira-Castro, Andreia
- Constante, Marco
- Magalhães, Marina
- Magalhães, Paula
- Cerqueira, Joana
- Vale, José
- Passão, Vitorina
- Barbosa, Célia
- Robalo, Conceição
- Coutinho, Paula
- Barros, José
- Santos, Manuela M
- Sequeiros, Jorge
- Maciel, Patrícia
Producer: 20061006
In:
Journal of human genetics vol. 51
Availability: No items available.
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507.
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510.
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511.
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Altered cochlear fibrocytes in a mouse model of DFN3 nonsyndromic deafness. [electronic resource] by
- Minowa, O
- Ikeda, K
- Sugitani, Y
- Oshima, T
- Nakai, S
- Katori, Y
- Suzuki, M
- Furukawa, M
- Kawase, T
- Zheng, Y
- Ogura, M
- Asada, Y
- Watanabe, K
- Yamanaka, H
- Gotoh, S
- Nishi-Takeshima, M
- Sugimoto, T
- Kikuchi, T
- Takasaka, T
- Noda, T
Producer: 19990914
In:
Science (New York, N.Y.) vol. 285
Availability: No items available.
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518.
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519.
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520.
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