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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1978 1
2014 2
2015 1
2016 1
2018 1
2021 2
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7 results
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Page 1
Intronic splicing mutations in PTCH1 cause Gorlin syndrome.
Bholah Z, Smith MJ, Byers HJ, Miles EK, Evans DG, Newman WG. Bholah Z, et al. Among authors: byers hj. Fam Cancer. 2014 Sep;13(3):477-80. doi: 10.1007/s10689-014-9712-9. Fam Cancer. 2014. PMID: 24659465
Extended gene panel testing in lobular breast cancer.
van Veen EM, Evans DG, Harkness EF, Byers HJ, Ellingford JM, Woodward ER, Bowers NL, Wallace AJ, Howell SJ, Howell A, Lalloo F, Newman WG, Smith MJ. van Veen EM, et al. Among authors: byers hj. Fam Cancer. 2021 Mar 25. doi: 10.1007/s10689-021-00241-5. Online ahead of print. Fam Cancer. 2021. PMID: 33763779
High likelihood of actionable pathogenic variant detection in breast cancer genes in women with very early onset breast cancer.
Evans DG, van Veen EM, Byers HJ, Evans SJ, Burghel GJ, Woodward ER, Harkness EF, Eccles DM, Greville-Haygate SL, Ellingford JM, Bowers NL, Pereira M, Wallace AJ, Howell SJ, Howell A, Lalloo F, Newman WG, Smith MJ. Evans DG, et al. Among authors: byers hj. J Med Genet. 2021 Mar 23:jmedgenet-2020-107347. doi: 10.1136/jmedgenet-2020-107347. Online ahead of print. J Med Genet. 2021. PMID: 33758026 Free article.