檢索結果 - Goldgar, D

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

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

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

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

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

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Multipoint linkage analysis in neurofibromatosis type I: an international collaboration. 由 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 由 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 由 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 由 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 由 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 由 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. 由 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. 由 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? 由 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? 由 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. 由 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? 由 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 由 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... 由 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 由 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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