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Author/Creator Frebourg, T

2. BRAF screening as a low-cost effective strategy for simplifying HNPCC genetic testing. Issue 9 (1st September 2004)

Authors:
Domingo, E; Laiho, P; Ollikainen, M; Pinto, M; Wang, L; French, A J; Westra, J; Frebourg, T; Espín, E; Armengol, M; Hamelin, R; Yamamoto, H; Hofstra, R M W; Seruca, R; Lindblom, A; Peltomäki, P; Thibodeau, S N; Aaltonen, L A; Schwartz, S
Journal:
Journal of medical genetics
Issue:
Volume 41:Issue 9(2004)
Page Start:
664
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Cleft lip/palate and CDH1/E-cadherin mutations in families with hereditary diffuse gastric cancer. Issue 2 (14th April 2005)

Authors:
Frebourg, T; Oliveira, C; Hochain, P; Karam, R; Manouvrier, S; Graziadio, C; Vekemans, M; Hartmann, A; Baert-Desurmont, S; Alexandre, C; Lejeune Dumoulin, S; Marroni, C; Martin, C; Castedo, S; Lovett, M; Winston, J; Machado, J C; Attié, T; Jabs, E W; Cai, J
Journal:
Journal of medical genetics
Issue:
Volume 43:Issue 2(2006)
Page Start:
138
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. De novo presenilin 1 mutations are rare in clinically sporadic, early onset Alzheimer's disease cases. French Alzheimer's Disease Study Group. Issue 8 (August 1998)

Authors:
Dumanchin, C; Brice, A; Campion, D; Hannequin, D; Martin, C; Moreau, V; Agid, Y; Martinez, M; Clerget-Darpoux, F; Frebourg, T
Journal:
Journal of medical genetics
Issue:
Volume 35:Issue 8(1998)
Page Start:
672
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

6. Impact of the MDM2 SNP309 and p53 Arg72Pro polymorphism on age of tumour onset in Li-Fraumeni syndrome. Issue 6 (28th October 2005)

Authors:
Bougeard, G; Baert-Desurmont, S; Tournier, I; Vasseur, S; Martin, C; Brugieres, L; Chompret, A; Bressac-de Paillerets, B; Stoppa-Lyonnet, D; Bonaiti-Pellie, C; Frebourg, T
Journal:
Journal of medical genetics
Issue:
Volume 43:Issue 6(2006)
Page Start:
531
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

8. No effect of the α1-antichymotrypsin A allele in Alzheimer's disease. Issue 1 (1st July 1997)

Authors:
Didierjean, O; Martinez, M; Campion, D; Hannequin, D; Dubois, B; Martin, C; Puel, M; Anterion, C Thomas; Pasquier, F; Moreau, O; Babron, M C; Penet, C; Agid, Y; Clerget-Darpoux, F; Frebourg, T; Brice, A
Journal:
Journal of neurology, neurosurgery and psychiatry
Issue:
Volume 63:Issue 1(1997)
Page Start:
103
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

9. No founder effect in three novel Alzheimer's disease families with APP 717 Val-->Ile mutation. Clerget-darpoux. French Alzheimer's Disease Study Group. Issue 8 (August 1996)

Authors:
Campion, D; Brice, A; Hannequin, D; Charbonnier, F; Dubois, B; Martin, C; Michon, A; Penet, C; Bellis, M; Calenda, A; Martinez, M; Agid, Y; Clerget-Darpoux, F; Frebourg, T
Journal:
Journal of medical genetics
Issue:
Volume 33:Issue 8(1996)
Page Start:
661
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗