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2841.
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2843.
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2844.
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2845.
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2846.
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Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer. [electronic resource] by
- Miyaki, M
- Konishi, M
- Tanaka, K
- Kikuchi-Yanoshita, R
- Muraoka, M
- Yasuno, M
- Igari, T
- Koike, M
- Chiba, M
- Mori, T
Producer: 19971204
In:
Nature genetics vol. 17
Availability: No items available.
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2847.
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2848.
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2849.
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2850.
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Tumours from MSH2 mutation carriers show loss of MSH2 expression but many tumours from MLH1 mutation carriers exhibit weak positive MLH1 staining. [electronic resource] by
- Mangold, Elisabeth
- Pagenstecher, Constanze
- Friedl, Waltraut
- Fischer, Hans-Peter
- Merkelbach-Bruse, Sabine
- Ohlendorf, Maike
- Friedrichs, Nicolaus
- Aretz, Stefan
- Buettner, Reinhard
- Propping, Peter
- Mathiak, Micaela
Producer: 20060113
In:
The Journal of pathology vol. 207
Availability: No items available.
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2851.
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2857.
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2858.
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Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome. [electronic resource] by
- van der Klift, Heleen M
- Mensenkamp, Arjen R
- Drost, Mark
- Bik, Elsa C
- Vos, Yvonne J
- Gille, Hans J J P
- Redeker, Bert E J W
- Tiersma, Yvonne
- Zonneveld, José B M
- García, Encarna Gómez
- Letteboer, Tom G W
- Olderode-Berends, Maran J W
- van Hest, Liselotte P
- van Os, Theo A
- Verhoef, Senno
- Wagner, Anja
- van Asperen, Christi J
- Ten Broeke, Sanne W
- Hes, Frederik J
- de Wind, Niels
- Nielsen, Maartje
- Devilee, Peter
- Ligtenberg, Marjolijn J L
- Wijnen, Juul T
- Tops, Carli M J
Producer: 20171107
In:
Human mutation vol. 37
Availability: No items available.
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2859.
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Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome. [electronic resource] by
- Hansen, Maren F
- Johansen, Jostein
- Sylvander, Anna E
- Bjørnevoll, Inga
- Talseth-Palmer, Bente A
- Lavik, Liss A S
- Xavier, Alexandre
- Engebretsen, Lars F
- Scott, Rodney J
- Drabløs, Finn
- Sjursen, Wenche
Producer: 20180516
In:
Clinical genetics vol. 92
Availability: No items available.
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2860.
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