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32621.
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32622.
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32632.
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Role of the BRAF mutations in the microsatellite instability genetic pathway in sporadic colorectal cancer. [electronic resource] by
- Maestro, M L
- Vidaurreta, M
- Sanz-Casla, M T
- Rafael, S
- Veganzones, S
- Martínez, A
- Aguilera, C
- Herranz, M D
- Cerdán, J
- Arroyo, M
Producer: 20070612
In:
Annals of surgical oncology vol. 14
Availability: No items available.
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32633.
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Identification of the Slynar gene (AY070435) and related brain expressed sequences as a candidate gene for susceptibility to affective disorders through allelic and haplotypic association with bipolar disorder on chromosome 12q24. [electronic resource] by
- Kalsi, Gursharan
- McQuillin, Andrew
- Degn, Birte
- Lundorf, Mikkel D
- Bass, Nicholas J
- Lawrence, Jacob
- Choudhury, Khalid
- Puri, Vinay
- Nyegaard, Mette
- Curtis, David
- Mors, Ole
- Kruse, Torben
- Kerwin, Simon
- Gurling, Hugh
Producer: 20061106
In:
The American journal of psychiatry vol. 163
Availability: No items available.
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32634.
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L-2-hydroxyglutaric aciduria: characterisation of the molecular defect in a spontaneous canine model. [electronic resource] by
- Penderis, Jacques
- Calvin, Jacqui
- Abramson, Carley
- Jakobs, Cornelis
- Pettitt, Louise
- Binns, Matthew M
- Verhoeven, Nanda M
- O'Driscoll, Eamonn
- Platt, Simon R
- Mellersh, Cathryn S
Producer: 20070521
In:
Journal of medical genetics vol. 44
Availability: No items available.
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32635.
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32636.
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32637.
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An autosome-wide scan for linkage disequilibrium-based association in sporadic breast cancer cases in eastern Finland: three candidate regions found. [electronic resource] by
- Hartikainen, Jaana M
- Tuhkanen, Hanna
- Kataja, Vesa
- Dunning, Alison M
- Antoniou, Antonis
- Smith, Paula
- Arffman, Airi
- Pirskanen, Mia
- Easton, Douglas F
- Eskelinen, Matti
- Uusitupa, Matti
- Kosma, Veli-Matti
- Mannermaa, Arto
Producer: 20050420
In:
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology vol. 14
Availability: No items available.
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32638.
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Overrepresentation of the founder PPOX gene mutation R59W in a South African patient with severe clinical manifestation of porphyria. [electronic resource] by
- de Villiers, J Nico P
- Kotze, Maritha J
- van Heerden, Carel J
- Sadie, Annalene
- Gardner, Helena F J
- Liebenberg, Juanita
- van Zyl, René
- du Plessis, Lana
- Kimberg, Matti
- Frank, Jorge
- Warnich, Louise
Producer: 20050822
In:
Experimental dermatology vol. 14
Availability: No items available.
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32639.
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32640.
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