Results
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25821.
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25822.
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25823.
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25824.
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25825.
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25826.
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25827.
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25828.
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25829.
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25830.
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Fine mapping of the multiple sclerosis susceptibility locus on 5p14-p12. [electronic resource] by
- Riise Stensland, Hilde Monica F
- Saarela, Janna
- Bronnikov, Denis O
- Parkkonen, Maija
- Jokiaho, Anne J
- Palotie, Aarno
- Tienari, Pentti J
- Sumelahti, Marja-Liisa
- Elovaara, Irina
- Koivisto, Keijo
- Pirttilä, Tuula
- Reunanen, Mauri
- Sobel, Eric
- Peltonen, Leena
Producer: 20060214
In:
Journal of neuroimmunology vol. 170
Availability: No items available.
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25831.
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25832.
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Microduplication and triplication of 22q11.2: a highly variable syndrome. [electronic resource] by
- Yobb, Twila M
- Somerville, Martin J
- Willatt, Lionel
- Firth, Helen V
- Harrison, Karen
- MacKenzie, Jennifer
- Gallo, Natasha
- Morrow, Bernice E
- Shaffer, Lisa G
- Babcock, Melanie
- Chernos, Judy
- Bernier, Francois
- Sprysak, Kathy
- Christiansen, Jesse
- Haase, Shelagh
- Elyas, Basil
- Lilley, Margaret
- Bamforth, Steven
- McDermid, Heather E
Producer: 20050616
In:
American journal of human genetics vol. 76
Availability: No items available.
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25833.
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25834.
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RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosa. [electronic resource] by
- Moore, A
- Escudier, E
- Roger, G
- Tamalet, A
- Pelosse, B
- Marlin, S
- Clément, A
- Geremek, M
- Delaisi, B
- Bridoux, A-M
- Coste, A
- Witt, M
- Duriez, B
- Amselem, S
Producer: 20060616
In:
Journal of medical genetics vol. 43
Availability: No items available.
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25835.
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25836.
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25837.
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25838.
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25839.
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25840.
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