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	1.	In situ carcinoma - can we predict which patient will come back with a recurrence? [electronic resource] by Simpson, Peter T Da Silva, Leonard M Lakhani, Sunil R Producer: 20071220 In: Cancer cell vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Bayes analysis provides evidence of pathogenicity for the BRCA1 c.135-1G>T (IVS3-1) and BRCA2 c.7977-1G>C (IVS17-1) variants displaying in vitro splicing results of equivocal clinical significance. [electronic resource] by Spurdle, Amanda B Lakhani, Sunil R Da Silva, Leonard M Balleine, Rosemary L Goldgar, David E Producer: 20100422 In: Human mutation vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Clinical classification of BRCA1 and BRCA2 DNA sequence variants: the value of cytokeratin profiles and evolutionary analysis--a report from the kConFab Investigators. [electronic resource] by Spurdle, Amanda B Lakhani, Sunil R Healey, Sue Parry, Suzanne Da Silva, Leonard M Brinkworth, Ross Hopper, John L Brown, Melissa A Babikyan, Davit Chenevix-Trench, Georgia Tavtigian, Sean V Goldgar, David E Producer: 20080513 In: Journal of clinical oncology : official journal of the American Society of Clinical Oncology vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Splicing and multifactorial analysis of intronic BRCA1 and BRCA2 sequence variants identifies clinically significant splicing aberrations up to 12 nucleotides from the intron/exon boundary. [electronic resource] by Whiley, Phillip J Guidugli, Lucia Walker, Logan C Healey, Sue Thompson, Bryony A Lakhani, Sunil R Da Silva, Leonard M Tavtigian, Sean V Goldgar, David E Brown, Melissa A Couch, Fergus J Spurdle, Amanda B Producer: 20110919 In: Human mutation vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Detection of splicing aberrations caused by BRCA1 and BRCA2 sequence variants encoding missense substitutions: implications for prediction of pathogenicity. [electronic resource] by Walker, Logan C Whiley, Phillip J Couch, Fergus J Farrugia, Daniel J Healey, Sue Eccles, Diana M Lin, Feng Butler, Samantha A Goff, Sheila A Thompson, Bryony A Lakhani, Sunil R Da Silva, Leonard M Tavtigian, Sean V Goldgar, David E Brown, Melissa A Spurdle, Amanda B Producer: 20100927 In: Human mutation vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)