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The BRCA2 c.68-7T > A variant is not pathogenic: A model fo..:
Colombo, M
;
Lòpez-Perolio, I
;
Meeks, HD
...
Human mutation, 2018, 39 (5), pp. 729 - 741. , 2019
Link:
https://repository.icr.ac.uk/handle/internal/3000
RT Journal T1
The BRCA2 c.68-7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity
UL https://suche.suub.uni-bremen.de/peid=base-ftinstcancerres:oai:repository.icr.ac.uk:internal_3000&Exemplar=1&LAN=DE A1 Colombo, M A1 Lòpez-Perolio, I A1 Meeks, HD A1 Caleca, L A1 Parsons, MT A1 Li, H A1 De Vecchi, G A1 Tudini, E A1 Foglia, C A1 Mondini, P A1 Manoukian, S A1 Behar, R A1 Garcia, EBG A1 Meindl, A A1 Montagna, M A1 Niederacher, D A1 Schmidt, AY A1 Varesco, L A1 Wappenschmidt, B A1 Bolla, MK A1 Dennis, J A1 Michailidou, K A1 Wang, Q A1 Aittomäki, K A1 Andrulis, IL A1 Anton-Culver, H A1 Arndt, V A1 Beckmann, MW A1 Beeghly-Fadel, A A1 Benitez, J A1 Boeckx, B A1 Bogdanova, NV A1 Bojesen, SE A1 Bonanni, B A1 Brauch, H A1 Brenner, H A1 Burwinkel, B A1 Chang-Claude, J A1 Conroy, DM A1 Couch, FJ A1 Cox, A A1 Cross, SS A1 Czene, K A1 Devilee, P A1 Dörk, T A1 Eriksson, M A1 Fasching, PA A1 Figueroa, J A1 Fletcher, O A1 Flyger, H A1 Gabrielson, M A1 García-Closas, M A1 Giles, GG A1 González-Neira, A A1 Guénel, P A1 Haiman, CA A1 Hall, P A1 Hamann, U A1 Hartman, M A1 Hauke, J A1 Hollestelle, A A1 Hopper, JL A1 Jakubowska, A A1 Jung, A A1 Kosma, V-M A1 Lambrechts, D A1 Le Marchand, L A1 Lindblom, A A1 Lubinski, J A1 Mannermaa, A A1 Margolin, S A1 Miao, H A1 Milne, RL A1 Neuhausen, SL A1 Nevanlinna, H A1 Olson, JE A1 Peterlongo, P A1 Peto, J A1 Pylkäs, K A1 Sawyer, EJ A1 Schmidt, MK A1 Schmutzler, RK A1 Schneeweiss, A A1 Schoemaker, MJ A1 See, MH A1 Southey, MC A1 Swerdlow, A A1 Teo, SH A1 Toland, AE A1 Tomlinson, I A1 Truong, T A1 van Asperen, CJ A1 van den Ouweland, AMW A1 van der Kolk, LE A1 Winqvist, R A1 Yannoukakos, D A1 Zheng, W A1 kConFab/AOCS Investigators A1 Dunning, AM A1 Easton, DF A1 Henderson, A A1 Hogervorst, FBL A1 Izatt, L A1 Offitt, K A1 Side, LE A1 van Rensburg, EJ A1 Embrace, S A1 Hebon, S A1 McGuffog, L A1 Antoniou, AC A1 Chenevix-Trench, G A1 Spurdle, AB A1 Goldgar, DE A1 Hoya, MDL A1 Radice, P YR 2019 K1 kConFab/AOCS Investigators K1 Cell Line K1 Humans K1 Genetic Predisposition to Disease K1 Mitomycin K1 BRCA2 Protein K1 RNA K1 Messenger K1 Calibration K1 RNA Splicing K1 Base Sequence K1 Exons K1 Models K1 Genetic K1 Female K1 Genetic Variation JF Human mutation, 2018, 39 (5), pp. 729 - 741 LK http://dx.doi.org/https://repository.icr.ac.uk/handle/internal/3000 DO https://repository.icr.ac.uk/handle/internal/3000 SF ELIB - SuUB Bremen
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