Výsledky vyhledávání - Goldgar, D

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

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

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

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

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

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

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No germline mutations in CDKN2A (p16) in patients with squamous cell cancer of the head and neck and second primary tumours Autor Jefferies, S, Edwards, S M, Hamoudi, R A, A'Hern, R, Foulkes, W, Goldgar, D, Eeles, R

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Dinucleotide repeat polymorphism at the D17S513 locus Autor Oliphant, A.R., Wright, E.C., Swensen, J., Gruis, N.A., Goldgar, D., Skolnick, M.H.

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Dinucleotide repeat polymorphism at the D17S514 locus Autor Oliphant, A.R., Wright, E.C., Swensen, J., Gruis, N.A., Goldgar, D., Skolnick, M.H.

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Colorectal tumour BRAF V600E and MLH1 promoter methylation status in the assessment of mismatch repair gene sequence variants of unknown clinical significance Autor Parsons, M, Thompson, B, Goldgar, D, Hopper, J, Jenkins, M, Buchanan, D, Young, J, Spurdle, A

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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 Autor 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. Autor Fain, P R, Goldgar, D E, Wallace, M R, Collins, F S, Wright, E, Nguyen, K, Barker, D F

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Genetic heterogeneity of breast-ovarian cancer revisited. Breast Cancer Linkage Consortium. Autor Narod, S, Ford, D, Devilee, P, Barkardottir, R B, Eyfjord, J, Lenoir, G, Serova, O, Easton, D, Goldgar, D

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An Alu-mediated 6-kb duplication in the BRCA1 gene: a new founder mutation? Autor Puget, N, Sinilnikova, O M, Stoppa-Lyonnet, D, Audoynaud, C, Pagès, S, Lynch, H T, Goldgar, D, Lenoir, G M, Mazoyer, S

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Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome? Autor 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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A genomic search for linkage of neurofibromatosis to RFLPs. Autor Barker, D, Wright, E, Nguyen, K, Cannon, L, Fain, P, Goldgar, D, Bishop, D T, Carey, J, Kivlin, J, Willard, H

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Mutations in BRCA1 and BRCA2 in breast cancer families: are there more breast cancer-susceptibility genes? Autor Serova, O M, Mazoyer, S, Puget, N, Dubois, V, Tonin, P, Shugart, Y Y, Goldgar, D, Narod, S A, Lynch, H T, Lenoir, G M

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Evidence for interaction between the TCO and NMTC1 loci in familial non-medullary thyroid cancer Autor McKay, J, Thompson, D, Lesueur, F, Stankov, K, Pastore, A, Watfah, C, Strolz, S, Riccabona, G, Moncayo, R, Romeo, G, Goldgar, D

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Prevalence and parental origin of de novo RET mutations in multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma. Le Groupe d'Etude des Tumeurs a Calcitonin... Autor Schuffenecker, I, Ginet, N, Goldgar, D, Eng, C, Chambe, B, Boneu, A, Houdent, C, Pallo, D, Schlumberger, M, Thivolet, C, Lenoir, G M

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The challenges of finding the gene responsible for a rare, autosomal dominant gastric cancer susceptibility syndrome Autor Li, JJ, Healey, S, Phillips, K, Makunin, I, Wayte, N, Schrader, I, Worthley, D, Lindor, N, Huntsman, D, Goldgar, D, Suthers, G, Chenevix-Trench, G

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