File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1002/humu.21628
- Scopus: eid_2-s2.0-84857691697
- PMID: 21990146
- WOS: WOS:000300705300002
Supplementary
- Citations:
- Appears in Collections:
Article: ENIGMA - evidence-based network for the interpretation of germline mutant alleles: an international initiative to evaluate risk and clinical significance associated with sequence variation in BRCA1 and BRCA2 genes
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Spurdle, AB | en_US |
dc.contributor.author | Healey, S | en_US |
dc.contributor.author | Devereau, A | en_US |
dc.contributor.author | Hogervorst, FB | en_US |
dc.contributor.author | Monteiro, AN | en_US |
dc.contributor.author | Nathanson, KL | en_US |
dc.contributor.author | Radice, P | en_US |
dc.contributor.author | Stoppa-Lyonnet, D | en_US |
dc.contributor.author | Tavtigian, S | en_US |
dc.contributor.author | Wappenschmidt, B | en_US |
dc.contributor.author | Couch, FJ | en_US |
dc.contributor.author | Pertesi, M | en_US |
dc.contributor.author | Cornell, M | en_US |
dc.contributor.author | Rouleau, E | en_US |
dc.contributor.author | Sharan, S | en_US |
dc.contributor.author | Rahman, N | en_US |
dc.contributor.author | Lalloo, F | en_US |
dc.contributor.author | Weitzel, J | en_US |
dc.contributor.author | Campbell, J | en_US |
dc.contributor.author | Cummings, | en_US |
dc.contributor.author | Machakova, E | en_US |
dc.contributor.author | Goldgar, DE | en_US |
dc.contributor.author | Olopade, F | en_US |
dc.contributor.author | Godwin, A | en_US |
dc.contributor.author | Ozcelik, H | en_US |
dc.contributor.author | Seminara, D | en_US |
dc.contributor.author | Goldgar, D | en_US |
dc.contributor.author | Couch, F | en_US |
dc.contributor.author | Fackenthal, JD | en_US |
dc.contributor.author | Thomassen, M | en_US |
dc.contributor.author | Teo, SH | en_US |
dc.contributor.author | Hansen, TV | en_US |
dc.contributor.author | Borg, A | en_US |
dc.contributor.author | Eeles, R | en_US |
dc.contributor.author | Toland, A | en_US |
dc.contributor.author | Rogan, P | en_US |
dc.contributor.author | Hansen, TV | en_US |
dc.contributor.author | Guidugli, L | en_US |
dc.contributor.author | Brody, LC | en_US |
dc.contributor.author | Healey, S | en_US |
dc.contributor.author | Brown, M | en_US |
dc.contributor.author | Kwong, A | en_US |
dc.contributor.author | Lei-po, CW | en_US |
dc.contributor.author | Nevanlinna, H | en_US |
dc.contributor.author | Garber, J | en_US |
dc.contributor.author | Foretova, L | en_US |
dc.contributor.author | Singer, CF | en_US |
dc.contributor.author | Blok, MJ | en_US |
dc.contributor.author | Spurdle, AB | en_US |
dc.contributor.author | Osorio, A | en_US |
dc.contributor.author | Kote-Jarai, Z | en_US |
dc.contributor.author | Wappenschmidt, B | en_US |
dc.contributor.author | Baralle, D | en_US |
dc.contributor.author | Vega, A | en_US |
dc.contributor.author | Blanco, A | en_US |
dc.contributor.author | Santamarina, M | en_US |
dc.contributor.author | Fachal, L | en_US |
dc.contributor.author | Nederlof, P | en_US |
dc.contributor.author | Peock, S | en_US |
dc.contributor.author | Pasini, B | en_US |
dc.contributor.author | Tommasi, S | en_US |
dc.contributor.author | Lafferty, A | en_US |
dc.contributor.author | Arisari, A | en_US |
dc.contributor.author | Konstantopoulou, I | en_US |
dc.contributor.author | Pal, T | en_US |
dc.contributor.author | Simard, J | en_US |
dc.contributor.author | Bonetti, A | en_US |
dc.contributor.author | Voresco, L | en_US |
dc.contributor.author | Peissel, B | en_US |
dc.contributor.author | Evans, DG | en_US |
dc.contributor.author | Foulkes, W | en_US |
dc.contributor.author | Szabo, C | en_US |
dc.contributor.author | van Asperen, C | en_US |
dc.contributor.author | Jonkers, J | en_US |
dc.contributor.author | Walker, L | en_US |
dc.contributor.author | Mitchell, G | en_US |
dc.contributor.author | Gutierrez-Enriquez, S | en_US |
dc.contributor.author | Diez, O | en_US |
dc.contributor.author | Millot, G | en_US |
dc.contributor.author | Fostira, F | en_US |
dc.contributor.author | Selkirk, C | en_US |
dc.contributor.author | Antoniou, A | en_US |
dc.contributor.author | Monteiro, A | en_US |
dc.contributor.author | Carvalho, M | en_US |
dc.contributor.author | Rubinstein, WS | en_US |
dc.contributor.author | de la Hoya, M | en_US |
dc.contributor.author | Domchek, S | en_US |
dc.contributor.author | Caputo, S | en_US |
dc.contributor.author | Houdayer, C | en_US |
dc.contributor.author | Blanco, I | en_US |
dc.contributor.author | Lazaro, C | en_US |
dc.contributor.author | Whiley, P | en_US |
dc.contributor.author | Becker, A | en_US |
dc.contributor.author | Aretini, P | en_US |
dc.contributor.author | Eccles, D | en_US |
dc.contributor.author | Caides, T | en_US |
dc.contributor.author | Viel, A | en_US |
dc.contributor.author | Izatt, L | en_US |
dc.contributor.author | Hogervorst, F | en_US |
dc.contributor.author | Radice, P | en_US |
dc.contributor.author | Nathanson, K | en_US |
dc.contributor.author | Pedersen, IS | en_US |
dc.contributor.author | Vreeswijk, M | en_US |
dc.contributor.author | Neuhausen, S | en_US |
dc.contributor.author | Yannoukakos, K | en_US |
dc.contributor.author | Tucker, K | en_US |
dc.contributor.author | Southey, M | en_US |
dc.contributor.author | Leary, J | en_US |
dc.contributor.author | Caligo, MA | en_US |
dc.contributor.author | Garcia, EG | en_US |
dc.contributor.author | Devereau, A | en_US |
dc.contributor.author | Brandao, R | en_US |
dc.contributor.author | Lidereau, R | en_US |
dc.contributor.author | Montagna, M | en_US |
dc.date.accessioned | 2012-04-24T07:53:18Z | - |
dc.date.available | 2012-04-24T07:53:18Z | - |
dc.date.issued | 2012 | en_US |
dc.identifier.citation | Human Mutation, 2012, v. 33 n. 1, p. 2-7 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/146428 | - |
dc.language | eng | en_US |
dc.relation.ispartof | Human Mutation | en_US |
dc.subject | BRCA1/BRCA2 | - |
dc.subject | Consortium | - |
dc.subject | International collaboration | - |
dc.subject | Unclassified variant | - |
dc.title | ENIGMA - evidence-based network for the interpretation of germline mutant alleles: an international initiative to evaluate risk and clinical significance associated with sequence variation in BRCA1 and BRCA2 genes | en_US |
dc.type | Article | en_US |
dc.identifier.email | Kwong, A: avakwong@hkucc.hku.hk | en_US |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1002/humu.21628 | - |
dc.identifier.pmid | 21990146 | - |
dc.identifier.scopus | eid_2-s2.0-84857691697 | - |
dc.identifier.hkuros | 199324 | en_US |
dc.identifier.volume | 33 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.spage | 2 | en_US |
dc.identifier.epage | 7 | en_US |
dc.identifier.isi | WOS:000300705300002 | - |