Results
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5601.
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5602.
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5603.
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5604.
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5605.
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5606.
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Congenital Achromatopsia and Macular Atrophy Caused by a Novel Recessive PDE6C Mutation (p.E591K). [electronic resource] by
- Katagiri, Satoshi
- Hayashi, Takaaki
- Yoshitake, Kazutoshi
- Sergeev, Yuri
- Akahori, Masakazu
- Furuno, Masaaki
- Nishino, Jo
- Ikeo, Kazuho
- Tsunoda, Kazushige
- Tsuneoka, Hiroshi
- Iwata, Takeshi
Producer: 20160223
In:
Ophthalmic genetics vol. 36
Availability: No items available.
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5607.
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5608.
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5609.
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5610.
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5611.
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Human rod monochromacy: linkage analysis and mapping of a cone photoreceptor expressed candidate gene on chromosome 2q11. [electronic resource] by
- Wissinger, B
- Jägle, H
- Kohl, S
- Broghammer, M
- Baumann, B
- Hanna, D B
- Hedels, C
- Apfelstedt-Sylla, E
- Randazzo, G
- Jacobson, S G
- Zrenner, E
- Sharpe, L T
Producer: 19981005
In:
Genomics vol. 51
Availability: No items available.
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5612.
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5613.
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5614.
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5615.
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5617.
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5620.
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