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Author/Creator Mangold, E

2. Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families. Issue 4 (1st April 2001)

Authors:
Friedl, W; Caspari, R; Sengteller, M; Uhlhaas, S; Lamberti, C; Jungck, M; Kadmon, M; Wolf, M; Fahnenstich, J; Gebert, J; Möslein, G; Mangold, E; Propping, P
Journal:
Gut
Issue:
Volume 48:Issue 4(2001)
Page Start:
515
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Defective removal of ribonucleotides from DNA promotes systemic lupus erythematosus. Issue 1 (December 2015)

Authors:
Günther, C; Kind, B; Reijns, MAM; Berndt, N; Martinez-Bueno, M; Wolf, C; Tüngler, V; Chara, O; Lee, YA; Hübner, N; Lee, YA; Bicknell, L; Blum, S; Krug, C; Schmidt, F; Krug, C; Kretschmer, S; Koss, S; Astell, KR; Ramantani, G
Journal:
Pediatric rheumatology online journal
Issue:
Volume 13:Issue 1(2015)
Page Start:
1
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. Defective removal of ribonucleotides from DNA promotes systemic lupus erythematosus. Issue 1 (December 2015)

Authors:
Günther, C; Kind, B; Reijns, MAM; Berndt, N; Martinez-Bueno, M; Wolf, C; Tüngler, V; Chara, O; Lee, YA; Hübner, N; Lee, YA; Bicknell, L; Blum, S; Krug, C; Schmidt, F; Krug, C; Kretschmer, S; Koss, S; Astell, KR; Ramantani, G
Journal:
Pediatric rheumatology online journal
Issue:
Volume 13:Issue 1(2015)
Page Start:
1
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

8. The MSH2 c.388_389del mutation shows a founder effect in Portuguese Lynch syndrome families. (27th December 2012)

Authors:
Pinheiro, M; Pinto, C; Peixoto, A; Veiga, I; Mesquita, B; Henrique, R; Lopes, P; Sousa, O; Fragoso, M; Dias, LM; Baptista, M; Marinho, C; Mangold, E; Vaccaro, C; Evans, DG; Farrington, S; Dunlop, MG; Teixeira, MR
Journal:
Clinical genetics
Issue:
Volume 84:Number 3(2013:Sep.)
Page Start:
244
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

9. The p53 codon 72 variation is associated with the age of onset of hereditary non-polyposis colorectal cancer (HNPCC). Issue 10 (30th September 2005)

Authors:
Krüger, S; Bier, A; Engel, C; Mangold, E; Pagenstecher, C; von Knebel Doeberitz, M; Holinski-Feder, E; Moeslein, G; Schulmann, K; Plaschke, J; Rüschoff, J; Schackert, H K
Other Names:
group-author.
Journal:
Journal of medical genetics
Issue:
Volume 42:Issue 10(2005)
Page Start:
769
Record Type:
Journal Article
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