Search Results - Goldgar, D

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  1. 1
    Multipoint analysis of human quantitative genetic variation.

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

    Published 1990
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  2. 2
    Comparison of a multipoint identity-by-descent method with parametric multipoint linkage analysis for mapping quantitative traits.

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

    Published 1992
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  3. 3
    Optimal strategies for mapping complex diseases in the presence of multiple loci.

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

    Published 1997
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  4. 4
    Models of multilocus recombination: nonrandomness in chiasma number and crossover positions.

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

    Published 1988
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  5. 5
    Bayesian interval estimation of genetic relationships: application to paternity testing.

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

    Published 1988
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  6. 6
    Multipoint linkage analysis in neurofibromatosis type I: an international collaboration.

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

    Published 1989
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  7. 7
    No germline mutations in CDKN2A (p16) in patients with squamous cell cancer of the head and neck and second primary tumours

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

    Published 2001
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  8. 8
    Dinucleotide repeat polymorphism at the D17S513 locus

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

    Published 1991
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  9. 9
    Dinucleotide repeat polymorphism at the D17S514 locus

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

    Published 1991
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  10. 10
    Colorectal tumour BRAF V600E and MLH1 promoter methylation status in the assessment of mismatch repair gene sequence variants of unknown clinical significance

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

    Published 2012
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  11. 11
    Assessing biases of information contained in pedigrees for the classification of BRCA-genetic variants: a study arising from the ENIGMA analytical working group

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

    Published 2016
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  12. 12
    Refined physical and genetic mapping of the NF1 region on chromosome 17.

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

    Published 1989
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  13. 13
    Genetic heterogeneity of breast-ovarian cancer revisited. Breast Cancer Linkage Consortium.

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

    Published 1995
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  14. 14
    An Alu-mediated 6-kb duplication in the BRCA1 gene: a new founder mutation?

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

    Published 1999
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  15. 15
    Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome?

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

    Published 1992
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  16. 16
    A genomic search for linkage of neurofibromatosis to RFLPs.

    A genomic search for linkage of neurofibromatosis to RFLPs. by Barker, D, Wright, E, Nguyen, K, Cannon, L, Fain, P, Goldgar, D, Bishop, D T, Carey, J, Kivlin, J, Willard, H

    Published 1987
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  17. 17
    Mutations in BRCA1 and BRCA2 in breast cancer families: are there more breast cancer-susceptibility genes?

    Mutations in BRCA1 and BRCA2 in breast cancer families: are there more breast cancer-susceptibility genes? by 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

    Published 1997
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  18. 18
    Evidence for interaction between the TCO and NMTC1 loci in familial non-medullary thyroid cancer

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

    Published 2004
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  19. 19
    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 Calcitonine.

    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... by Schuffenecker, I, Ginet, N, Goldgar, D, Eng, C, Chambe, B, Boneu, A, Houdent, C, Pallo, D, Schlumberger, M, Thivolet, C, Lenoir, G M

    Published 1997
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  20. 20
    The challenges of finding the gene responsible for a rare, autosomal dominant gastric cancer susceptibility syndrome

    The challenges of finding the gene responsible for a rare, autosomal dominant gastric cancer susceptibility syndrome by 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

    Published 2012
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