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Volumn 101, Issue 1, 1997, Pages 102-108

Eighteen new polymorphic markers in the multiple endocrine neoplasia type 1 (MEN1) region

Author keywords

[No Author keywords available]

Indexed keywords

DNA MARKER;

EID: 0031438435     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050595     Document Type: Article
Times cited : (58)

References (29)
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  • 11
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    • Fine scale mapping of the gene responsible for multiple endocrine neoplasia type 1 (MEN1)
    • Fujimori M, Wells SA, Nakamura Y (1992) Fine scale mapping of the gene responsible for multiple endocrine neoplasia type 1 (MEN1). Am J Hum Genet 50 : 399-403
    • (1992) Am J Hum Genet , vol.50 , pp. 399-403
    • Fujimori, M.1    Wells, S.A.2    Nakamura, Y.3
  • 15
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    • Multiple endocrine neoplasia type 1 maps to chromosome 11 and is lost in insulinoma
    • Larsson C, Skogseid B, Oberg K, Nakamura Y, Nordenskjold M (1988) Multiple endocrine neoplasia type 1 maps to chromosome 11 and is lost in insulinoma. Nature 332 : 85-87
    • (1988) Nature , vol.332 , pp. 85-87
    • Larsson, C.1    Skogseid, B.2    Oberg, K.3    Nakamura, Y.4    Nordenskjold, M.5
  • 16
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    • Bardet-Beidl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneous
    • Leppert M, Baird L, Anderson KL, Otterud B, Lupski JR, Lewis RA (1994) Bardet-Beidl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneous. Nat Genet 7 : 108-111
    • (1994) Nat Genet , vol.7 , pp. 108-111
    • Leppert, M.1    Baird, L.2    Anderson, K.L.3    Otterud, B.4    Lupski, J.R.5    Lewis, R.A.6
  • 18
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    • Analysis of a second family with hereditary non-chromaffin paragangliomas locates the underlying gene at the proximal region of chromosome 11q
    • Mariman ECM, Beersum SEC van, Cremers CWRJ, Baars FM van, Ropers HH (1993) Analysis of a second family with hereditary non-chromaffin paragangliomas locates the underlying gene at the proximal region of chromosome 11q. Hum Genet 91 : 357-361
    • (1993) Hum Genet , vol.91 , pp. 357-361
    • Mariman, E.C.M.1    Van Beersum, S.E.C.2    Cremers, C.W.R.J.3    Van Baars, F.M.4    Ropers, H.H.5
  • 22
    • 0028360153 scopus 로고
    • Mapping the gene for hereditary hyperparathyroidism and prolactinoma (MENl-Burin) to chromosome 11q: Evidence for a founder effect in patients from Newfoundland
    • Petty EM, Green JS, Marx SJ, Taggart RT, Farid N, Bale AE (1994) Mapping the gene for hereditary hyperparathyroidism and prolactinoma (MENl-Burin) to chromosome 11q: evidence for a founder effect in patients from Newfoundland. Am J Hum Genet 54 : 1060-1066
    • (1994) Am J Hum Genet , vol.54 , pp. 1060-1066
    • Petty, E.M.1    Green, J.S.2    Marx, S.J.3    Taggart, R.T.4    Farid, N.5    Bale, A.E.6
  • 23
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    • Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11
    • Ranum LPW, Schut LJ, Lundgren JK, Orr HT, Livingston DM (1994) Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11. Nat Genet 8 : 280-284
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    • Ranum, L.P.W.1    Schut, L.J.2    Lundgren, J.K.3    Orr, H.T.4    Livingston, D.M.5
  • 25
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    • Linkage of vitelliform macular degereration (Best's disease) to chromosome 11q13
    • Stone EM, Nichols BE, Streb LM, Kimura AE, Sheffield VC (1992a) Linkage of vitelliform macular degereration (Best's disease) to chromosome 11q13. Nat Genet 1 : 246-250
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.