Proliferative compartment deregulation in the non-neoplastic colonic epithelium of familial adenomatous polyposis.

Por Mills, S J, Shepherd, N A, Hall, P A, Hastings, A, Mathers, J C, Gunn, A
Publicado em 1995

The impact of whole genome sequence data on drug discovery--a malaria case study.

Por Joachimiak, M. P., Chang, C., Rosenthal, P. J., Cohen, F. E.
Publicado em 2001

Joint action on monitoring injuries in Europe (JAMIE)

Por Rogmans, W H J
Publicado em 2012

On Genome-wide Association Studies for Family-Based Designs: An Integrative Analysis Approach Combining Ascertained Family Samples with Unselected Controls

Por Lasky-Su, Jessica, Won, Sungho, Mick, Eric, Anney, Richard J.L., Franke, Barbara, Neale, Benjamin, Biederman, Joseph, Smalley, Susan L., Loo, Sandra K., Todorov, Alexandre, Faraone, Stephen V., Weiss, Scott T., Lange, Christoph
Publicado em 2010

Medullary thyroid carcinoma in Northern Ireland, 1967-1997.

Por Dolan, S. J., Russell, C. F.
Publicado em 2000

The seroprevalence of antithyroid peroxidase antibodies in bipolar families and bipolar twins: results from two longitudinal studies

Por Snijders, G., de Witte, L., Mesman, E., Kemner, S., Vonk, R., Brouwer, R., Nolen, W. A., Drexhage, H. A., Hillegers, M. H. J.
Publicado no Int J Bipolar Disord (2017)

Evaluation of mammographic surveillance services in women aged 40–49 years with a moderate family history of breast cancer: a single-arm cohort study

Por SW Duffy, J Mackay, S Thomas, E Anderson, THH Chen, I Ellis, G Evans, H Fielder, R Fox, G Gui, D Macmillan, S Moss, C Rogers, M Sibbering, M Wallis, R Warren, E Watson, D Whynes, P Allgood, J Caunt
Publicado em 2013-03-01

Evaluation of mammographic surveillance services in women aged 40-49 years with a moderate family history of breast cancer: a single-arm cohort study.

Por Duffy, S W, Mackay, J, Thomas, S, Anderson, E, Chen, T H H, Ellis, I, Evans, G, Fielder, H, Fox, R, Gui, G, Macmillan, D, Moss, S, Rogers, C, Sibbering, M, Wallis, M, Warren, R, Watson, E, Whynes, D, Allgood, P, Caunt, J
Publicado no Health Technol Assess (2013)

Genotypic diagnosis of familial Mediterranean fever (FMF) using new microsatellite markers: example of two extensive non-Ashkenazi Jewish pedigrees.

Por Dupont, M, Dross, C, Smaoui, N, Nedelec, B, Grateau, G, Clépet, C, Gourdier, I, Koné-Paut, I, Delpech, M, Demaille, J, Touitou, I
Publicado em 1997

Extended associative memories

Por J.H Sossa Azuela, R. Barrón Fernández
Publicado no Revista Mexicana de Física (2007)

Contact-induced language in the Western Amazon : the non-genetic origin of the Kokama language /

Por Cabral, Ana Suelly Arruda Câmara, Chamberlain, Bobby J.
Publicado em 1995

Somatic hypermutation and B-cell lymphoma.

Por Dunn-Walters, D, Thiede, C, Alpen, B, Spencer, J
Publicado em 2001

Matrix metalloproteinase 13 activity is associated with poor prognosis in colorectal cancer

Por Leeman, M F, McKay, J A, Murray, G I
Publicado em 2002

Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international study.

Por Neuhausen, S. L., Mazoyer, S., Friedman, L., Stratton, M., Offit, K., Caligo, A., Tomlinson, G., Cannon-Albright, L., Bishop, T., Kelsell, D., Solomon, E., Weber, B., Couch, F., Struewing, J., Tonin, P., Durocher, F., Narod, S., Skolnick, M. H., Lenoir, G., Serova, O., Ponder, B., Stoppa-Lyonnet, D., Easton, D., King, M. C., Goldgar, D. E.
Publicado em 1996

Targeting MARCO can lead to enhanced dendritic cell motility and anti-melanoma activity

Por Matsushita, Norimasa, Komine, Hiroshi, Grolleau-Julius, Annabelle, Pilon-Thomas, Shari, Mulé, James J.
Publicado em 2010

Information provision for stroke patients and their caregivers

Por Forster, Anne, Brown, Lesley, Smith, Jane, House, Allan, Knapp, Peter, Wright, John J, Young, John
Publicado no Cochrane Database Syst Rev (2012)

D-TRANSPOSITION OF THE GREAT ARTERIES: Hot Topics in the Current Era of the Arterial Switch Operation

Por Villafañe, Juan, Lantin-Hermoso, M. Regina, Bhatt, Ami B., Tweddell, James S., Geva, Tal, Nathan, Meena, Elliott, Martin J., Vetter, Victoria L., Paridon, Stephen M., Kochilas, Lazaros, Jenkins, Kathy J., Beekman, Robert H., Wernovsky, Gil, Towbin, Jeffrey A.
Publicado no J Am Coll Cardiol (2014)

Impact of genetic counselling after neonatal screening for Duchenne muscular dystrophy.

Por Hildes, E, Jacobs, H K, Cameron, A, Seshia, S S, Booth, F, Evans, J A, Wrogemann, K, Greenberg, C R
Publicado em 1993

Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era

Por Norton, Nadine, Robertson, Peggy D., Rieder, Mark J., Zuchner, Stephan, Rampersaud, Evadnie, Martin, Eden, Li, Duanxiang, Nickerson, Deborah A., Hershberger, Ray E.
Publicado em 2012

Promoter methylation of candidate genes associated with familial testicular cancer

Por Mirabello, Lisa, Kratz, Christian P, Savage, Sharon A, Greene, Mark H
Publicado em 2012