Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

729 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Women's attitudes toward preventive strategies for hereditary breast or ovarian carcinoma differ from one country to another: differences among English, French, and Canadian women.
Julian-Reynier CM, Bouchard LJ, Evans DG, Eisinger FA, Foulkes WD, Kerr B, Blancquaert IR, Moatti JP, Sobol HH. Julian-Reynier CM, et al. Among authors: kerr b. Cancer. 2001 Aug 15;92(4):959-68. doi: 10.1002/1097-0142(20010815)92:4<959::aid-cncr1406>3.0.co;2-v. Cancer. 2001. PMID: 11550171
Fictitious breast cancer family history.
Evans DG, Kerr B, Cade D, Hoare E, Hopwood P. Evans DG, et al. Among authors: kerr b. Lancet. 1996 Oct 12;348(9033):1034. doi: 10.1016/S0140-6736(05)64963-X. Lancet. 1996. PMID: 8855883 No abstract available.
Neurofibromatosis type 1 and sporadic optic gliomas.
Singhal S, Birch JM, Kerr B, Lashford L, Evans DG. Singhal S, et al. Among authors: kerr b. Arch Dis Child. 2002 Jul;87(1):65-70. doi: 10.1136/adc.87.1.65. Arch Dis Child. 2002. PMID: 12089128 Free PMC article.
Weaver syndrome and EZH2 mutations: Clarifying the clinical phenotype.
Tatton-Brown K, Murray A, Hanks S, Douglas J, Armstrong R, Banka S, Bird LM, Clericuzio CL, Cormier-Daire V, Cushing T, Flinter F, Jacquemont ML, Joss S, Kinning E, Lynch SA, Magee A, McConnell V, Medeira A, Ozono K, Patton M, Rankin J, Shears D, Simon M, Splitt M, Strenger V, Stuurman K, Taylor C, Titheradge H, Van Maldergem L, Temple IK, Cole T, Seal S; Childhood Overgrowth Consortium; Rahman N. Tatton-Brown K, et al. Am J Med Genet A. 2013 Dec;161A(12):2972-80. doi: 10.1002/ajmg.a.36229. Epub 2013 Nov 8. Am J Med Genet A. 2013. PMID: 24214728 Free article.
An absence of cutaneous neurofibromas associated with a 3-bp inframe deletion in exon 17 of the NF1 gene (c.2970-2972 delAAT): evidence of a clinically significant NF1 genotype-phenotype correlation.
Upadhyaya M, Huson SM, Davies M, Thomas N, Chuzhanova N, Giovannini S, Evans DG, Howard E, Kerr B, Griffiths S, Consoli C, Side L, Adams D, Pierpont M, Hachen R, Barnicoat A, Li H, Wallace P, Van Biervliet JP, Stevenson D, Viskochil D, Baralle D, Haan E, Riccardi V, Turnpenny P, Lazaro C, Messiaen L. Upadhyaya M, et al. Among authors: kerr b. Am J Hum Genet. 2007 Jan;80(1):140-51. doi: 10.1086/510781. Epub 2006 Dec 8. Am J Hum Genet. 2007. PMID: 17160901 Free PMC article.
BRCA1/2 predictive testing: a study of uptake in two centres.
Brooks L, Lennard F, Shenton A, Lalloo F, Ambus I, Ardern-Jones A, Belk R, Kerr B, Craufurd D, Eeles R, Gareth Evans D. Brooks L, et al. Among authors: kerr b. Eur J Hum Genet. 2004 Aug;12(8):654-62. doi: 10.1038/sj.ejhg.5201206. Eur J Hum Genet. 2004. PMID: 15138457
729 results