نتائج البحث - Goldgar, D E

Multipoint analysis of human quantitative genetic variation. حسب Goldgar, D E

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Comparison of a multipoint identity-by-descent method with parametric multipoint linkage analysis for mapping quantitative traits. حسب Goldgar, D E, Oniki, R S

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Optimal strategies for mapping complex diseases in the presence of multiple loci. حسب Goldgar, D E, Easton, D F

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Models of multilocus recombination: nonrandomness in chiasma number and crossover positions. حسب Goldgar, D E, Fain, P R

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Bayesian interval estimation of genetic relationships: application to paternity testing. حسب Goldgar, D E, Thompson, E A

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Multipoint linkage analysis in neurofibromatosis type I: an international collaboration. حسب Goldgar, D E, Green, P, Parry, D M, Mulvihill, J J

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Assessing biases of information contained in pedigrees for the classification of BRCA-genetic variants: a study arising from the ENIGMA analytical working group حسب Kerkhofs, C. H. H., Spurdle, A. B., Lindsey, P. J., Goldgar, D. E., Gómez-García, E. B.

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Refined physical and genetic mapping of the NF1 region on chromosome 17. حسب Fain, P R, Goldgar, D E, Wallace, M R, Collins, F S, Wright, E, Nguyen, K, Barker, D F

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Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome? حسب Stern, H J, Saal, H M, Lee, J S, Fain, P R, Goldgar, D E, Rosenbaum, K N, Barker, D F

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Chromosome 17q linkage studies of 18 Utah breast cancer kindreds. حسب Goldgar, D E, Cannon-Albright, L A, Oliphant, A, Ward, J H, Linker, G, Swensen, J, Tran, T D, Fields, P, Uharriet, P, Skolnick, M H

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Evidence against the reported linkage of the cutaneous melanoma-dysplastic nevus syndrome locus to chromosome Ip36. حسب Cannon-Albright, L A, Goldgar, D E, Wright, E C, Turco, A, Jost, M, Meyer, L J, Piepkorn, M, Zone, J J, Skolnick, M H

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Cancer risks in two large breast cancer families linked to BRCA2 on chromosome 13q12-13. حسب Easton, D F, Steele, L, Fields, P, Ormiston, W, Averill, D, Daly, P A, McManus, R, Neuhausen, S L, Ford, D, Wooster, R, Cannon-Albright, L A, Stratton, M R, Goldgar, D E

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Familial nontoxic multinodular thyroid goiter locus maps to chromosome 14q but does not account for familial nonmedullary thyroid cancer. حسب Bignell, G R, Canzian, F, Shayeghi, M, Stark, M, Shugart, Y Y, Biggs, P, Mangion, J, Hamoudi, R, Rosenblatt, J, Buu, P, Sun, S, Stoffer, S S, Goldgar, D E, Romeo, G, Houlston, R S, Narod, S A, Stratton, M R, Foulkes, W D

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Cannabis, tobacco and domestic fumes intake are associated with nasopharyngeal carcinoma in North Africa حسب Feng, B-J, Khyatti, M, Ben-Ayoub, W, Dahmoul, S, Ayad, M, Maachi, F, Bedadra, W, Abdoun, M, Mesli, S, Bakkali, H, Jalbout, M, Hamdi-Cherif, M, Boualga, K, Bouaouina, N, Chouchane, L, Benider, A, Ben-Ayed, F, Goldgar, D E, Corbex, M

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

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Rare Mutations in XRCC2 Increase the Risk of Breast Cancer حسب Park, D.J., Lesueur, F., Nguyen-Dumont, T., Pertesi, M., Odefrey, F., Hammet, F., Neuhausen, S.L., John, E.M., Andrulis, I.L., Terry, M.B., Daly, M., Buys, S., Le Calvez-Kelm, F., Lonie, A., Pope, B.J., Tsimiklis, H., Voegele, C., Hilbers, F.M., Hoogerbrugge, N., Barroso, A., Osorio, A., Giles, G.G., Devilee, P., Benitez, J., Hopper, J.L., Tavtigian, S.V., Goldgar, D.E., Southey, M.C.

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Tumour morphology predicts PALB2 germline mutation status حسب Teo, Z L, Provenzano, E, Dite, G S, Park, D J, Apicella, C, Sawyer, S D, James, P A, Mitchell, G, Trainer, A H, Lindeman, G J, Shackleton, K, Cicciarelli, L, Buys, S S, Andrulis, I L, Mulligan, A M, Glendon, G, John, E M, Terry, M B, Daly, M, Odefrey, F A, Nguyen-Dumont, T, Giles, G G, Dowty, J G, Winship, I, Goldgar, D E, Hopper, J L, Southey, M C

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Multigene testing of moderate-risk genes: be mindful of the missense حسب Young, E L, Feng, B J, Stark, A W, Damiola, F, Durand, G, Forey, N, Francy, T C, Gammon, A, Kohlmann, W K, Kaphingst, K A, McKay-Chopin, S, Nguyen-Dumont, T, Oliver, J, Paquette, A M, Pertesi, M, Robinot, N, Rosenthal, J S, Vallee, M, Voegele, C, Hopper, J L, Southey, M C, Andrulis, I L, John, E M, Hashibe, M, Gertz, J, Le Calvez-Kelm, F, Lesueur, F, Goldgar, D E, Tavtigian, S V

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Breast-Cancer Risk in Families with Mutations in PALB2 حسب Antoniou, A.C., Casadei, S., Heikkinen, T., Barrowdale, D., Pylkäs, K., Roberts, J., Lee, A., Subramanian, D., De Leeneer, K., Fostira, F., Tomiak, E., Neuhausen, S.L., Teo, Z.L., Khan, S., Aittomäki, K., Moilanen, J.S., Turnbull, C., Seal, S., Mannermaa, A., Kallioniemi, A., Lindeman, G.J., Buys, S.S., Andrulis, I.L., Radice, P., Tondini, C., Manoukian, S., Toland, A.E., Miron, P., Weitzel, J.N., Domchek, S.M., Poppe, B., Claes, K.B.M., Yannoukakos, D., Concannon, P., Bernstein, J.L., James, P.A., Easton, D.F., Goldgar, D.E., Hopper, J.L., Rahman, N., Peterlongo, P., Nevanlinna, H., King, M.-C., Couch, F.J., Southey, M.C., Winqvist, R., Foulkes, W.D., Tischkowitz, M.

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