Does Lymphedema Severity Affect Quality of Life? Simple Question. Challenging Answers von Lee, Teresa S, Morris, Carol M, Czerniec, Sharon A, Mangion, Andrea J

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Multicentric breast cancer: clonality and prognostic studies von Eeles, R., Knee, G., Jhavar, S., Mangion, J., Ebbs, S., Gui, G., Thomas, S., Coppen, M., A’Hern, R., Gray, S., Cooper, C., Bartek, J., Yarnold, J.

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Localization of a Breast Cancer Susceptibility Gene, BRCA2, to Chromosome 13q12-13 von Wooster, Richard, Neuhausen, Susan L., Mangion, Jonathan, Quirk, Yvette, Ford, Deborah, Collins, Nadine, Nguyen, Kim, Seal, Sheila, Tran, Thao, Averill, Diane, Fields, Patty, Marshall, Gill, Narod, Steven, Lenoir, Gilbert M., Lynch, Henry, Feunteun, Jean, Devilee, Peter, Cornelisse, Cees J., Menko, Fred H., Daly, Peter A., Ormiston, Wilma, McManus, Ross, Pye, Carole, Lewis, Cathryn M., Cannon-Albright, Lisa A., Peto, Julian, Bruce A. J. Ponder, Skolnick, Mark H., Easton, Douglas F., Goldgar, David E., Stratton, Michael R.

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Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans von Domin, Jan, Mangion, Jonathan, Cook, H. Terence, Petretto, Enrico, Vyse, Timothy J, Flint, Jonathan, Johnson, Michelle D, Patel, Sheetal G, Pusey, Charles D, Cook, Paul R, Evans, David J, Duda, Mark, Smith, Jennifer, Dong, Rong, Bhangal, Gurjeet, Aitman, Timothy J, Roberton-Lowe, Cheri, Sheehan-Rooney, Kelly, Marshall, Amy J, Boyle, Joseph J, Norsworthy, Penny J, Hodges, Matthew D

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Instability of short tandem repeats (microsatellites) in human cancers von Wooster, R, Cleton-Jansen, A.-M, Collins, N, Mangion, J, Cornelis, R.S, Cooper, C.S, Gusterson, B.A, Ponder, B.A.J, von Deimling, A, Wiestler, O.D, Cornelisse, C.J, Devilee, P, Stratton, M.R

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Screening hCHK2 for mutations von Sodha, N, Williams, R, Mangion, J, Bullock, S L, Yuille, M R, Eeles, R A

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Diphtheria in Europe von Mangion, J. P., Mancini, S., Bachy, C., de Weggheleire, A., Zamatto, F.

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Inherited susceptibility to colorectal adenomas and carcinomas: Evidence for a new predisposition gene on 15q14-q22 von Tomlinson, Ian, Rahman, Nazneen, Frayling, Ian, Mangion, Jon, Barfoot, Rita, Hamoudi, Rifat, Seal, Sheila, Northover, John, Thomas, Huw J.W., Neale, Kay, Hodgson, Shirley, Talbot, Ian, Houlston, Richard, Stratton, Michael R.

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[401] IMPACT OF MULTIPLE TREATMENT INTERRUPTIONS ON VIRUS-HOST INTERACTIONS IN HBeAg-POSITIVE CHRONIC HEPATITIS B (CHB) von Chokshi, S, Petretto, E, Cooksley, H, Mangion, J, Hill, J, Naoumov, N.V

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Molecular characterization of mitochondrial apoptosis-inducing factor von Kroemer, Guido, Susin, Santos A, Lorenzo, Hans K, Zamzami, Naoufal, Marzo, Isabel, Snow, Bryan E, Brothers, Greg M, Mangion, Joan, Jacotot, Etienne, Costantini, Paola, Loeffler, Markus, Larochette, Nathanael, Goodlett, David R, Aebersold, Ruedi, Siderovski, David P, Penninger, Josef M

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Low-penetrance susceptibility to breast cancer due to CHEK21100delC in noncarriers of BRCA1 or BRCA2 mutations von Meijers-Heijboer, Hanne, van den Ouweland, Ans, Klijn, Jan, Wasielewski, Marijke, de Snoo, Anja, Oldenburg, Rogier, Hollestelle, Antoinette, Houben, Mark, Crepin, Ellen, van Veghel-Plandsoen, Monique, Elstrodt, Fons, van Duijn, Cornelia, Bartels, Carina, Meijers, Carel, Schutte, Mieke, McGuffog, Lesley, Thompson, Deborah, Easton, Douglas F, Sodha, Nayanta, Seal, Sheila, Barfoot, Rita, Mangion, Jon, Chang-Claude, Jenny, Eccles, Diana, Eeles, Rosalind, Evans, D Gareth, Houlston, Richard, Murday, Victoria, Narod, Steven, Peretz, Tamara, Peto, Julian, Phelan, Catherine, Zhang, Hong Xiang, Szabo, Csilla, Devilee, Peter, Goldgar, David, Futreal, P Andrew, Nathanson, Katherine L, Weber, Barbara L, Rahman, Nazneen, Stratton, Michael R

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A patient-based self-examination survey for staging the severity of lymphoedema von Morris, Carol M, Lee, Teresa S, Czerniec, Sharon A, Mangion, Andrea J

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A Gene for Lymphedema-Distichiasis Maps to 16q24.3 von Mangion, J., Rahman, N., Mansour, S., Brice, G., Rosbotham, J., Child, A.H., Murday, V.A., Mortimer, P.S., Barfoot, R., Sigurdsson, A., Edkins, S., Sarfarazi, M., Burnand, K., Evans, A.L., Nunan, T.O., Stratton, M.R., Jeffery, S.

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BRCA1 and BRCA2 germline mutations in Sardinian breast cancer families and their implications for genetic counseling von Palmieri, G., Palomba, G., Cossu, A., Pisano, M., Dedola, M. F., Sarobba, M. G., Farris, A., Olmeo, N., Contu, A., Pasca, A., Satta, M. P., Persico, I., Carboni, A. A., Cossu-Rocca, P., Contini, M., Mangion, J., Stratton, M. R., Tanda, F.

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Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease von Hocking, Lynne J., Lucas, Gavin J.A., Daroszewska, Anna, Mangion, Jon, Olavesen, Mark, Cundy, Tim, Nicholson, Geoff C., Ward, Lynley, Bennett, Simon T., Wuyts, Wim, Van Hul, Wim, Ralston, Stuart H.

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Linkage and LOH studies in 19 cylindromatosis families show no evidence of genetic heterogeneity and refine the CYLD locus on chromosome 16q12-q13 von TAKAHASHI, M, RAPLEY, E, EVANS, D. G, SCHRANDER-STUMPEL, C, BEEMER, F. A, VAN VLOTEN, W. A, BREUNING, M. H, VAN DEN OUWELAND, A, HALLEY, D, DELPECH, B, CLEVELAND, M, LEIGH, I, BIGGS, P. J, CHAPMAN, P, BURN, J, HOHL, D, GÖRÖG, J.-P, SEAL, S, MANGION, J, WARREN, W, BIGNELL, G, STRATTON, M. R, LAKHANI, S. R, COOKE, D, HANSEN, J, BLAIR, E, HOFMANN, B, SIEBERT, R, TURNER, G

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Familial craniofacial fibrous dysplasia: absence of linkage to GNAS1 and the gene for cherubism von Mangion, J, Edkins, S, Goss, A N, Stratton, M R, Flanagan, A M

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BAX frameshift mutations in cell lines derived from human haemopoietic malignancies are associated with resistance to apoptosis and microsatellite instability von BRIMMELL, M, MENDIOLA, R, MANGION, J, PACKHAM, G

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Large-scale analysis of association between polymorphisms in the transforming growth factor beta 1 gene (TGFB1) and osteoporosis: The GENOMOS study von Langdahl, Bente L, Uitterlinden, André G, Ralston, Stuart H, Trikalinos, Thomas A, Balcells, Susanne, Brandi, Maria Luisa, Scollen, Serena, Lips, Paul, Lorenc, Roman, Obermayer-Pietsch, Barbara, Reid, David M, Armas, Jácome Bruges, Arp, Pascal P, Bassiti, Amelia, Bustamante, Mariona, Husted, Lise Bjerre, Carey, Alison H, Pérez Cano, Ramon, Dobnig, Harald, Dunning, Alison M, Fahrleitner-Pammer, Astrid, Falchetti, Alberto, Karczmarewicz, Elzbieta, Kruk, Marcin, van Leeuwen, Johannes P.T.M, Masi, Laura, van Meurs, Joyce B.J, Mangion, Jon, McGuigan, Fiona E.A, Mellibovsky, Leonardo, Mosekilde, Leif, Nogués, Xavier, Pols, Huibert A.P, Reeve, Jonathan, Renner, Wilfried, Rivadeneira, Fernando, van Schoor, Natasja M, Ioannidis, John P.A

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Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene von Gayther, Simon A, Mangion, Jonathon, Russell, Paul, Seal, Sheila, Barfoot, Rita, Ponder, Bruce A.J, Stratton, Michael R, Easton, Douglas

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