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Journal Abstract Search

168 related items for PubMed ID: 1978560

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2B map to the same region of chromosome 10 as multiple endocrine neoplasia type 2A.
    Lairmore TC, Howe JR, Korte JA, Dilley WG, Aine L, Aine E, Wells SA, Donis-Keller H.
    Genomics; 1991 Jan; 9(1):181-92. PubMed ID: 1672289
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  • 3. A new DNA marker (D10S94) very tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locus.
    Goodfellow PJ, Myers S, Anderson LL, Brooks-Wilson AR, Simpson NE.
    Am J Hum Genet; 1990 Dec; 47(6):952-6. PubMed ID: 1978561
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  • 5. Linkage of the multiple endocrine neoplasia type 2B gene (MEN2B) to chromosome 10 markers linked to MEN2A.
    Norum RA, Lafreniere RG, O'Neal LW, Nikolai TF, Delaney JP, Sisson JC, Sobol H, Lenoir GM, Ponder BA, Willard HF.
    Genomics; 1990 Oct; 8(2):313-7. PubMed ID: 1979053
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  • 6. 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; 83(4):353-8. PubMed ID: 2572534
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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. 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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  • 10. Extensive sequence polymorphisms associated with chromosome 10 alpha satellite DNA and its close linkage to markers from the pericentromeric region.
    Wu JS, Kidd KK.
    Hum Genet; 1990 Feb 01; 84(3):279-82. PubMed ID: 1968036
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  • 11. Allele loss on chromosome 10 and point mutation of ras oncogenes are infrequent in tumors of MEN 2A.
    Okazaki M, Miya A, Tanaka N, Miki T, Yamamoto M, Motomura K, Miyauchi A, Mori T, Takai S.
    Henry Ford Hosp Med J; 1989 Feb 01; 37(3-4):112-5. PubMed ID: 2576939
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  • 13. The gene for MEN 2A is tightly linked to the centromere of chromosome 10.
    Narod SA, Sobol H, Schuffenecker I, Lavoué MF, Lenoir GM.
    Hum Genet; 1991 Mar 01; 86(5):529-30. PubMed ID: 1673115
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  • 15. Early detection of hereditary medullary thyroid cancer with polymorphic DNA probes. Groupe d'Etude des Tumeurs a Calcitonine.
    Narod SA, Sobol H, Schuffenecker I, Ezekowitz RA, Lenoir GM.
    Henry Ford Hosp Med J; 1989 Mar 01; 37(3-4):106-8. PubMed ID: 2576937
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  • 16. Multiple endocrine neoplasia, the old and the new: a mini review.
    Pasquali D, Di Matteo FM, Renzullo A, Accardo G, Esposito D, Barbato F, Colantuoni V, Circelli L, Conzo G.
    G Chir; 2012 Mar 01; 33(11-12):370-3. PubMed ID: 23140918
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  • 17. Closing in on the MEN2A locus.
    Simpson NE, Kidd KK.
    Henry Ford Hosp Med J; 1989 Mar 01; 37(3-4):100-5. PubMed ID: 2576936
    [Abstract] [Full Text] [Related]

  • 18. Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours.
    Eng C, Smith DP, Mulligan LM, Nagai MA, Healey CS, Ponder MA, Gardner E, Scheumann GF, Jackson CE, Tunnacliffe A.
    Hum Mol Genet; 1994 Feb 01; 3(2):237-41. PubMed ID: 7911697
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  • 20. Loss of genes on chromosome 22 in medullary thyroid carcinoma and pheochromocytoma.
    Takai S, Tateishi H, Nishisho I, Miki T, Motomura K, Miyauchi A, Kato M, Ikeuchi T, Yamamoto K, Okazaki M.
    Jpn J Cancer Res; 1987 Sep 01; 78(9):894-8. PubMed ID: 2889715
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