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45281.
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45282.
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45283.
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Molecular and clinical characterisation of three Spanish families with maternally inherited non-syndromic hearing loss caused by the 1494C->T mutation in the mitochondrial 12S rRNA gene. [electronic resource] by
- Rodríguez-Ballesteros, M
- Olarte, M
- Aguirre, L A
- Galán, F
- Galán, R
- Vallejo, L A
- Navas, C
- Villamar, M
- Moreno-Pelayo, M A
- Moreno, F
- del Castillo, I
Producer: 20061215
In:
Journal of medical genetics vol. 43
Availability: No items available.
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45284.
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Identification of 14 novel mutations in the long isoform of USH2A in Spanish patients with Usher syndrome type II. [electronic resource] by
- Aller, E
- Jaijo, T
- Beneyto, M
- Nájera, C
- Oltra, S
- Ayuso, C
- Baiget, M
- Carballo, M
- Antiñolo, G
- Valverde, D
- Moreno, F
- Vilela, C
- Collado, D
- Pérez-Garrigues, H
- Navea, A
- Millán, J M
Producer: 20061215
In:
Journal of medical genetics vol. 43
Availability: No items available.
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45285.
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45286.
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45287.
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45288.
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A proboscidean from the late Oligocene of Eritrea, a "missing link" between early Elephantiformes and Elephantimorpha, and biogeographic implications. [electronic resource] by
- Shoshani, Jeheskel
- Walter, Robert C
- Abraha, Michael
- Berhe, Seife
- Tassy, Pascal
- Sanders, William J
- Marchant, Gary H
- Libsekal, Yosief
- Ghirmai, Tesfalidet
- Zinner, Dietmar
Producer: 20070105
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 103
Availability: No items available.
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45289.
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45290.
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45291.
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45292.
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45293.
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45294.
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45295.
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45296.
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45297.
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45298.
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45299.
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45300.
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