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A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect. [electronic resource] by
- Thiselton, D L
- Alexander, C
- Morris, A
- Brooks, S
- Rosenberg, T
- Eiberg, H
- Kjer, B
- Kjer, P
- Bhattacharya, S S
- Votruba, M
Producer: 20011220
In:
Human genetics vol. 109
Availability: No items available.
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OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28. [electronic resource] by
- Alexander, C
- Votruba, M
- Pesch, U E
- Thiselton, D L
- Mayer, S
- Moore, A
- Rodriguez, M
- Kellner, U
- Leo-Kottler, B
- Auburger, G
- Bhattacharya, S S
- Wissinger, B
Producer: 20001108
In:
Nature genetics vol. 26
Availability: No items available.
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A region of 35 kb containing the trace amine associate receptor 6 (TAAR6) gene is associated with schizophrenia in the Irish study of high-density schizophrenia families. [electronic resource] by
- Vladimirov, V
- Thiselton, D L
- Kuo, P-H
- McClay, J
- Fanous, A
- Wormley, B
- Vittum, J
- Ribble, R
- Moher, B
- van den Oord, E
- O'Neill, F A
- Walsh, D
- Kendler, K S
- Riley, B P
Producer: 20071206
In:
Molecular psychiatry vol. 12
Availability: No items available.
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