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MSH6 mutation in Muir-Torre syndrome: could this be a rare finding? [electronic resource] by
- Mangold, E
- Rahner, N
- Friedrichs, N
- Buettner, R
- Pagenstecher, C
- Aretz, S
- Friedl, W
- Ruzicka, T
- Propping, P
- Rütten, A
- Kruse, R
Producer: 20070517
In:
The British journal of dermatology vol. 156
Availability: No items available.
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Gene transfer of the costimulatory molecules B7-1 and B7-2 into human multiple myeloma cells by recombinant adeno-associated virus enhances the cytolytic T cell response. [electronic resource] by
- Wendtner, C M
- Nolte, A
- Mangold, E
- Buhmann, R
- Maass, G
- Chiorini, J A
- Winnacker, E L
- Emmerich, B
- Kotin, R M
- Hallek, M
Producer: 19970919
In:
Gene therapy vol. 4
Availability: No items available.
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14.
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Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families. [electronic resource] by
- 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
Producer: 20010419
In:
Gut vol. 48
Availability: No items available.
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15.
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The p53 codon 72 variation is associated with the age of onset of hereditary non-polyposis colorectal cancer (HNPCC). [electronic resource] by
- 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
Producer: 20060724
In:
Journal of medical genetics vol. 42
Availability: No items available.
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16.
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Evidence for a polygenic contribution to androgenetic alopecia. [electronic resource] by
- Heilmann, S
- Brockschmidt, F F
- Hillmer, A M
- Hanneken, S
- Eigelshoven, S
- Ludwig, K U
- Herold, C
- Mangold, E
- Becker, T
- Kruse, R
- Knapp, M
- Nöthen, M M
Producer: 20140527
In:
The British journal of dermatology vol. 169
Availability: No items available.
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17.
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DHPLC mutation analysis of the hereditary nonpolyposis colon cancer (HNPCC) genes hMLH1 and hMSH2. [electronic resource] by
- Holinski-Feder, E
- Müller-Koch, Y
- Friedl, W
- Moeslein, G
- Keller, G
- Plaschke, J
- Ballhausen, W
- Gross, M
- Baldwin-Jedele, K
- Jungck, M
- Mangold, E
- Vogelsang, H
- Schackert, H K
- Lohsea, P
- Murken, J
- Meitinger, T
Producer: 20010521
In:
Journal of biochemical and biophysical methods vol. 47
Availability: No items available.
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18.
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Common variants in DLG1 locus are associated with non-syndromic cleft lip with or without cleft palate. [electronic resource] by
- Mostowska, A
- Gaczkowska, A
- Żukowski, K
- Ludwig, K U
- Hozyasz, K K
- Wójcicki, P
- Mangold, E
- Böhmer, A C
- Heilmann-Heimbach, S
- Knapp, M
- Zadurska, M
- Biedziak, B
- Budner, M
- Lasota, A
- Daktera-Micker, A
- Jagodziński, P P
Producer: 20190930
In:
Clinical genetics vol. 93
Availability: No items available.
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19.
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Frequency of hereditary non-polyposis colorectal cancer among unselected patients with colorectal cancer in Germany. [electronic resource] by
- Lamberti, C
- Mangold, E
- Pagenstecher, C
- Jungck, M
- Schwering, D
- Bollmann, M
- Vogel, J
- Kindermann, D
- Nikorowitsch, R
- Friedrichs, N
- Schneider, B
- Houshdaran, F
- Schmidt-Wolf, I G H
- Friedl, W
- Propping, P
- Sauerbruch, T
- Büttner, R
- Mathiak, M
Producer: 20070208
In:
Digestion vol. 74
Availability: No items available.
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20.
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The MSH2 c.388_389del mutation shows a founder effect in Portuguese Lynch syndrome families. [electronic resource] by
- Pinheiro, M
- Pinto, C
- Peixoto, A
- Veiga, I
- Mesquita, B
- Henrique, R
- Lopes, P
- Sousa, O
- Fragoso, M
- Dias, L M
- Baptista, M
- Marinho, C
- Mangold, E
- Vaccaro, C
- Evans, D G
- Farrington, S
- Dunlop, M G
- Teixeira, M R
Producer: 20140306
In:
Clinical genetics vol. 84
Availability: No items available.
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