Browse by Uncontrolled Keywords
Number of items: 9.
2009
Jones, N;
Vogt, S;
Nielsen, M;
Christian, D;
Wark, PA;
Eccles, D;
Edwards, E;
Evans, DG;
Maher, ER;
Vasen, HF;
+3 more...
Hes, FJ;
Aretz, S;
Sampson, JR;
(2009)
Increased Colorectal Cancer Incidence in Obligate Carriers of Heterozygous Mutations in MUTYH.
Gastroenterology, 137 (2).
pp. 489-494.
ISSN 0016-5085
DOI: https://doi.org/10.1053/j.gastro.2009.04.047
Full text not available from this repository.
2008
Reis-Filho, JS;
Drury, S;
Lambros, MB;
Marchio, C;
Johnson, N;
Natrajan, R;
Salter, J;
Levey, P;
Fletcher, O;
Peto, J;
+2 more...
Ashworth, A;
Dowsett, M;
(2008)
ESR1 gene amplification in breast cancer: a common phenomenon?
Nature genetics, 40 (7).
pp. 809-810.
ISSN 1061-4036
DOI: https://doi.org/10.1038/ng0708-809b
Full text not available from this repository.
2007
Alharbi, KK;
Spanakis, E;
Tan, K;
Smith, MJ;
Aldahmesh, MA;
O'Dell, SD;
Sayer, AA;
Lawlor, DA;
Ebrahim, S;
Smith, GD;
+5 more...
O'Rahilly, S;
Farooqi, S;
Cooper, C;
Phillips, DIW;
Day, INM;
(2007)
Prevalence and functionality of paucimorphic and private MC4R mutations in a large, unselected European British population, scanned by meltMADGE.
Human mutation, 28 (3).
pp. 294-302.
ISSN 1059-7794
DOI: https://doi.org/10.1002/humu.20404
Full text not available from this repository.
2006
Smith, R;
Raithatha, N;
(2006)
Why disclosure of genetic tests for health insurance should be voluntary.
Journal of health services research & policy, 11 (3).
pp. 184-6.
ISSN 1355-8196
DOI: https://doi.org/10.1258/135581906777641730
Full text not available from this repository.
2004
Raithatha, N;
Smith, RD;
(2004)
Disclosure of genetic tests for health insurance: is it ethical not to?
Lancet, 363 (9406).
pp. 395-6.
ISSN 0140-6736
DOI: https://doi.org/10.1016/S0140-6736(04)15442-1
Full text not available from this repository.
2002
Meijers-Heijboer, H;
van Den Ouweland, A;
Klijn, J;
Wasielewski, M;
de Snoo, A;
Oldenburg, R;
Hollestelle, A;
Houben, M;
Crepin, E;
van Veghel-Plandsoen, M;
+31 more...
Elstrodt, F;
van Duijn, C;
Bartels, C;
Meijers, C;
Schutte, M;
McGuffog, L;
Thompson, D;
Easton, DF;
Sodha, N;
Seal, S;
Barfoot, R;
Mangion, J;
Chang-Claude, J;
Eccles, D;
Eeles, R;
Evans, DG;
Houlston, R;
Murday, V;
Narod, S;
Peretz, T;
Peto, J;
Phelan, C;
Zhang, HX;
Szabo, C;
Devilee, P;
Goldgar, D;
Futreal, PA;
Nathanson, KL;
Weber, BL;
Rahman, N;
Stratton, MR;
(2002)
Low-penetrance susceptibility to breast cancer due to CHEK2*1100delC in noncarriers of BRCA1 or BRCA2 mutations.
Nature genetics, 31 (1).
pp. 55-59.
ISSN 1061-4036
DOI: https://doi.org/10.1038/ng879
Full text not available from this repository.
2001
Omar, SA;
Adagu, IS;
Warhurst, DC;
(2001)
Can pretreatment screening for dhps and dhfr point mutations in Plasmodium falciparum infections be used to predict sulfadoxine-pyrimethamine treatment failure?
Transactions of the Royal Society of Tropical Medicine and Hygiene, 95 (3).
pp. 315-9.
ISSN 0035-9203
https://researchonline.lshtm.ac.uk/id/eprint/16300
Full text not available from this repository.
Vineis, P;
Schulte, P;
McMichael, AJ;
(2001)
Misconceptions about the use of genetic tests in populations.
Lancet, 357 (9257).
pp. 709-12.
ISSN 0140-6736
DOI: https://doi.org/10.1016/S0140-6736(00)04136-2
Full text not available from this repository.
Whitwell, JL;
Crum, WR;
Watt, HC;
Fox, NC;
(2001)
Normalization of cerebral volumes by use of intracranial volume: implications for longitudinal quantitative MR imaging.
AJNR American journal of neuroradiology, 22 (8).
pp. 1483-9.
ISSN 0195-6108
https://researchonline.lshtm.ac.uk/id/eprint/15442
Full text not available from this repository.