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Journal Abstract Search

442 related items for PubMed ID: 1672289

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  • 4. The mutation for medullary thyroid carcinoma with parathyroid tumors (MTC with PTs) is closely linked to the centromeric region of chromosome 10.
    Carson NL, Wu JS, Jackson CE, Kidd KK, Simpson NE.
    Am J Hum Genet; 1990 Dec; 47(6):946-51. PubMed ID: 1978560
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  • 6. Hereditary medullary thyroid carcinoma: genetic annalysis of three related syndromes. Groupe d'Etude des Tumeurs a Calcitonine.
    Sobol H, Narod SA, Schuffenecker I, Amos C, Ezekowitz RA, Lenoir GM.
    Henry Ford Hosp Med J; 1989 Dec; 37(3-4):109-11. PubMed ID: 2576938
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  • 7. The genetic defect in multiple endocrine neoplasia type 2A maps next to the centromere of chromosome 10.
    Wu JS, Carson NL, Myers S, Pakstis AJ, Kidd JR, Castiglione CM, Anderson L, Hoyle LS, Genel M, Verdy M.
    Am J Hum Genet; 1990 Mar; 46(3):624-30. PubMed ID: 1968709
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  • 8. Genetics of the multiple endocrine neoplasia type 2B syndrome.
    Jackson CE, Norum RA.
    Henry Ford Hosp Med J; 1992 Mar; 40(3-4):232-5. PubMed ID: 1362412
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  • 9. A cluster of CpG islands at D10S94, near the locus responsible for multiple endocrine neoplasia type 2A (MEN2A).
    Brooks-Wilson AR, Smailus DE, Goodfellow PJ.
    Genomics; 1992 Jun; 13(2):339-43. PubMed ID: 1351867
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  • 10. Genomic and yeast artificial chromosome long-range physical maps linking six loci in 10q11.2 and spanning the multiple endocrine neoplasia type 2A (MEN2A) region.
    Brooks-Wilson AR, Lichter JB, Ward DC, Kidd KK, Goodfellow PJ.
    Genomics; 1993 Sep; 17(3):611-7. PubMed ID: 7902324
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  • 11.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Eng C, Plitt G.
    ; 1993 Sep. PubMed ID: 20301434
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  • 12. Low incidence of loss of chromosome 10 in sporadic and hereditary human medullary thyroid carcinoma.
    Nelkin BD, Nakamura Y, White RW, de Bustros AC, Herman J, Wells SA, Baylin SB.
    Cancer Res; 1989 Aug 01; 49(15):4114-9. PubMed ID: 2568166
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  • 13. A new polymorphic marker (D10S97) tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locus.
    Lichter JB, Wu J, Brooks-Wilson AR, Difillipantonio M, Brewster S, Ward DC, Goodfellow PJ, Kidd KK.
    Hum Genet; 1993 Jan 01; 90(5):516-20. PubMed ID: 8094065
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  • 14. Improved predictive test for MEN2, using flanking dinucleotide repeats and RFLPs.
    Howe JR, Lairmore TC, Mishra SK, Dou S, Veile R, Wells SA, Donis-Keller H.
    Am J Hum Genet; 1992 Dec 01; 51(6):1430-42. PubMed ID: 1361102
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  • 15. Linkage analysis of hereditary thyroid carcinoma with and without pheochromocytoma.
    Narod SA, Sobol H, Nakamura Y, Calmettes C, Baulieu JL, Bigorgne JC, Chabrier G, Couette J, de Gennes JL, Duprey J.
    Hum Genet; 1989 Nov 01; 83(4):353-8. PubMed ID: 2572534
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  • 16. Genetic linkage studies map the multiple endocrine neoplasia type 2 loci to a small interval on chromosome 10q11.2.
    Gardner E, Papi L, Easton DF, Cummings T, Jackson CE, Kaplan M, Love DR, Mole SE, Moore JK, Mulligan LM.
    Hum Mol Genet; 1993 Mar 01; 2(3):241-6. PubMed ID: 8098977
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  • 17. Linked markers flanking the gene for multiple endocrine neoplasia type 2A.
    Nakamura Y, Mathew CG, Sobol H, Easton DF, Telenius H, Bragg T, Chin K, Clark J, Jones C, Lenoir GM.
    Genomics; 1989 Aug 01; 5(2):199-203. PubMed ID: 2571570
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  • 18. Consistent association of 1p loss of heterozygosity with pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes.
    Moley JF, Brother MB, Fong CT, White PS, Baylin SB, Nelkin B, Wells SA, Brodeur GM.
    Cancer Res; 1992 Feb 15; 52(4):770-4. PubMed ID: 1346584
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  • 19. Genetic screening of endocrine tumour syndromes with DNA probes: the example of medullary thyroid carcinoma.
    Sobol H, Narod SA, Assouline D, Lenoir GM.
    Horm Res; 1989 Feb 15; 32(1-3):34-40. PubMed ID: 2575577
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  • 20. Genetic events in tumour initiation and progression in multiple endocrine neoplasia type 2.
    Mulligan LM, Gardner E, Smith BA, Mathew CG, Ponder BA.
    Genes Chromosomes Cancer; 1993 Mar 15; 6(3):166-77. PubMed ID: 7682102
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