Zobrazeno 1 - 4
of 4
pro vyhledávání: '"C. G. Norbury"'
Autor:
R. Davison, Claire Taylor, Rosalind A. Eeles, Ian Tomlinson, Mark Longmuir, Shirley Hodgson, Lara Lipton, Richard S. Houlston, Victoria Murday, Huw Thomas, C. G. Norbury
Publikováno v:
Familial Cancer. 1:189-195
It is not uncommon for cancer geneticists to be referred families with apparently Mendelian co-inheritance of breast and bowel cancer. Such families present a particular problem as regards the intensity of their screening for these diseases and the u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46bd28ab20d0942cb78539ea2477476e
https://doi.org/10.1023/a:1021101014264
https://doi.org/10.1023/a:1021101014264
Autor:
C G Norbury, R S Shiwach
Publikováno v:
British Journal of Psychiatry. 165:500-505
BackgroundThe study tested specific hypotheses that (a) there is an increased incidence of psychiatric disorders in asymptomatic heterozygotes for Huntington's disease (HD) compared with the normal homozygotes, and (b) there is an increased incidence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87a70ae501233acebc58d293785bf854
https://doi.org/10.1192/bjp.165.4.500
https://doi.org/10.1192/bjp.165.4.500
Autor:
L, Lipton, H J, Thomas, R A, Eeles, R S, Houlston, M, Longmuir, R, Davison, S V, Hodgson, V A, Murday, C G, Norbury, C, Taylor, I P, Tomlinson
Publikováno v:
Familial cancer. 1(3-4)
It is not uncommon for cancer geneticists to be referred families with apparently Mendelian co-inheritance of breast and bowel cancer. Such families present a particular problem as regards the intensity of their screening for these diseases and the u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::438a5327f23f3b3922cb1c722f05147d
https://pubmed.ncbi.nlm.nih.gov/14574178
https://pubmed.ncbi.nlm.nih.gov/14574178
Autor:
Sabine Tejpar, David Markie, K Neale, Jin Cheon Kim, G Evans, Richard S. Houlston, Kang Mo Kim, Kelly Woodford-Richens, Charis Eng, Devendra Desai, Walter F. Bodmer, B Dowling, I P M Tomlinson, Michael Churchman, Eamonn Sheridan, D. Eccles, Paul Rozen, Malcolm G. Dunlop, Barbara A. Leggett, C. G. Norbury, G T Smith, Miguel A. Rodriguez-Bigas, Takeo Iwama, Julian R. Sampson, R. K. S. Phillips, Daniel Jones, Shirley Hodgson, Steve Bevan, Joanne P. Young
Publikováno v:
Gut. 46(5)
BACKGROUND—Juvenile polyposis syndrome (JPS) is characterised by gastrointestinal (GI) hamartomatous polyposis and an increased risk of GI malignancy. Juvenile polyps also occur in the Cowden (CS), Bannayan-Ruvalcaba-Riley (BRRS) and Gorlin (GS) sy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87398d71d56761016443d1469e2ae532
http://ora.ox.ac.uk/objects/uuid:992c369d-f4aa-4c95-bc7d-9ec7d6aa8ca6
http://ora.ox.ac.uk/objects/uuid:992c369d-f4aa-4c95-bc7d-9ec7d6aa8ca6