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Entries: 1-3  
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SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype
Authors: Stoepker, C.; Hain, K.; Schuster, B.; Hilhorst-Hofstee, Y.; Rooimans, M. A.; Steltenpool, J.; Oostra, A. B.; Eirich, K.; Korthof, E. T.; Nieuwint, A. W. M.; Jaspers, N. G. J.; Bettecken, T.; Joenje, H.; Schindler, D.; Rouse, J.; de Winter, J. P.
Date of Publication (YYYY-MM-DD): 2011-02
Title of Journal: Nature Genetics
Volume: 43
Issue / Number: 2
Start Page: 138
End Page: 141
Document Type: Article
ID: 536127.0
Clinical variability and novel mutations in the NHEJ1 gene in patients with a Nijmegen breakage syndrome-like phenotype.
Authors: Dutrannoy, V.; Demuth, I.; Baumann, U.; Schindler, D.; Konrat, K.; Neitzel, H.; Gillessen-Kaesbach, G.; Radszewski, J.; Rothe, S.; Schellenberger, M. T.; Nurnberg, G.; Nurnberg, P.; Teik, K. W.; Nallusamy, R.; Reis, A.; Sperling, K.; Digweed, M.; Varon, R.
Date of Publication (YYYY-MM-DD): 2010-07-01
Title of Journal: Human Mutation
Volume: 31
Issue / Number: 9
Start Page: 1059
End Page: 1068
Document Type: Article
ID: 539705.0
Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene
Authors: Meindl, A.; Hellebrand, H.; Wiek, C.; Erven, V.; Wappenschmidt, B.; Niederacher, D.; Freund, M.; Lichtner, P.; Hartmann, L.; Schaal, H.; Ramser, J.; Honisch, E.; Kubisch, C.; Wichmann, H. E.; Kast, K.; Deissler, H.; Engel, C.; Müller-Myhsok, B.; Neveling, K.; Kiechle, M.; Mathew, C. G.; Schindler, D.; Schmutzler, R. K.; Hanenberg, H.
Date of Publication (YYYY-MM-DD): 2010-05
Title of Journal: Nature Genetics
Volume: 42
Issue / Number: 5
Start Page: 410
End Page: 414
Document Type: Article
ID: 477357.0
Entries: 1-3  
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