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Volumn 100, Issue 3-4, 1997, Pages 426-430

Localization of the gene for Wieacker-Wolff syndrome in the pericentromeric region of the X chromosome

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME XQ; GENE LOCATION; HUMAN; MALFORMATION SYNDROME; PRIORITY JOURNAL; X CHROMOSOME LINKAGE; X CHROMOSOME RECESSIVE INHERITANCE;

EID: 0030983979     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050528     Document Type: Article
Times cited : (13)

References (26)
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    • Allen, R.C.1    Belmont, J.W.2
  • 2
    • 0027304536 scopus 로고
    • Two simple repeat polymorphisms at DXS337
    • Barker DF, Nguyen K, Fain PR (1993) Two simple repeat polymorphisms at DXS337. Hum Mol Gent 2:1507
    • (1993) Hum Mol Gent , vol.2 , pp. 1507
    • Barker, D.F.1    Nguyen, K.2    Fain, P.R.3
  • 6
    • 0026952517 scopus 로고
    • Identification of a highly polymorphic marker within intron 7 of the ALAS2 gene and suggestion of at least two loci for sideroblastic anemia
    • Cox TC, Kozman HM, Raskind WH, May BK, Mulley JC (1992) Identification of a highly polymorphic marker within intron 7 of the ALAS2 gene and suggestion of at least two loci for sideroblastic anemia. Hum Mol Genet 8:639-641
    • (1992) Hum Mol Genet , vol.8 , pp. 639-641
    • Cox, T.C.1    Kozman, H.M.2    Raskind, W.H.3    May, B.K.4    Mulley, J.C.5
  • 9
    • 0027300467 scopus 로고
    • Dinucleotide repeat polymorphisms from DXS106 and DXS227 YACs using a stage approach
    • Fairweather N, Chelly J, Monaco AP (1993) Dinucleotide repeat polymorphisms from DXS106 and DXS227 YACs using a stage approach. Hum Mol Genet 2:607-608
    • (1993) Hum Mol Genet , vol.2 , pp. 607-608
    • Fairweather, N.1    Chelly, J.2    Monaco, A.P.3
  • 10
    • 0021908106 scopus 로고
    • X-linked dominant Charcot-Marie-Tooth disease: Suggestion of linkage with a cloned DNA sequence from the proximal Xq
    • Gal A, Mucke J, Theile H, Wieacker P, Ropers HH, Wienker TF (1985) X-linked dominant Charcot-Marie-Tooth disease: suggestion of linkage with a cloned DNA sequence from the proximal Xq. Hum Genet 70:38-42
    • (1985) Hum Genet , vol.70 , pp. 38-42
    • Gal, A.1    Mucke, J.2    Theile, H.3    Wieacker, P.4    Ropers, H.H.5    Wienker, T.F.6
  • 12
    • 0019193212 scopus 로고
    • Non-specific X-linked mental retardation, II. the frequency in British Columbia
    • Herbst DS, Miller JR (1980) Non-specific X-linked mental retardation, II. The frequency in British Columbia. Am J Med Genet 7:461-469
    • (1980) Am J Med Genet , vol.7 , pp. 461-469
    • Herbst, D.S.1    Miller, J.R.2
  • 13
    • 1842264097 scopus 로고
    • Linkage of the Wieacker-Wolff syndrome and a CAG-tandem repeat polymorphism within the androgen receptor gene
    • Jakubiczka S, Krawczak M, Nedel S, Wieacker P (1993) Linkage of the Wieacker-Wolff syndrome and a CAG-tandem repeat polymorphism within the androgen receptor gene. Med Genet 1:131
    • (1993) Med Genet , vol.1 , pp. 131
    • Jakubiczka, S.1    Krawczak, M.2    Nedel, S.3    Wieacker, P.4
  • 14
    • 1842352746 scopus 로고
    • No evidence for allelic heterogeneity in X-linked neural Charcot-Marie-Tooth disease (CMTX) and Wieacker-Wolff syndrome
    • Jakubiczka S, Nedel S, Wieacker P (1995) No evidence for allelic heterogeneity in X-linked neural Charcot-Marie-Tooth disease (CMTX) and Wieacker-Wolff syndrome. Med Genet 2:211
    • (1995) Med Genet , vol.2 , pp. 211
    • Jakubiczka, S.1    Nedel, S.2    Wieacker, P.3
  • 17
    • 0026025786 scopus 로고
    • Unique X-linked mental retardation syndrome with fingertip arches and contractures linked to Xq21.31
    • Miles JH, Carpenter NJ (1991) Unique X-linked mental retardation syndrome with fingertip arches and contractures linked to Xq21.31. Am J Med Genet 38:215-223
    • (1991) Am J Med Genet , vol.38 , pp. 215-223
    • Miles, J.H.1    Carpenter, N.J.2
  • 18
    • 0000036322 scopus 로고
    • A simple salting out procedure for extracting DNA from human nucleated cells
    • Miller SA, Dykes DD, Polesky HF (1988) A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 19:6968
    • (1988) Nucleic Acids Res , vol.19 , pp. 6968
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  • 22
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    • Linkage studies with the gene for an X-linked syndrome of mental retardation, microcephaly and spastic diplegia (MRX2)
    • Sutherland GR, Gedeon AK, Haan EA, Woodroffe P, Mulley JC (1988) Linkage studies with the gene for an X-linked syndrome of mental retardation, microcephaly and spastic diplegia (MRX2). Am J Med Genet 30:493-508
    • (1988) Am J Med Genet , vol.30 , pp. 493-508
    • Sutherland, G.R.1    Gedeon, A.K.2    Haan, E.A.3    Woodroffe, P.4    Mulley, J.C.5
  • 24
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    • Wieacker P, Wolff G, Wienker TF, Sauer M (1985) A new X-linked syndrome with muscle atrophy, congenital contractures, and oculomotor apraxia. Am J Med Genet 20:597-606
    • (1985) Am J Med Genet , vol.20 , pp. 597-606
    • Wieacker, P.1    Wolff, G.2    Wienker, T.F.3    Sauer, M.4
  • 25
    • 0023630581 scopus 로고
    • Close linkage of the Wieacker-Wolff syndrome to the DNA, segment DXYS1 in proximal Xq
    • Wieacker P, Wolff G, Wienker TF (1987) Close linkage of the Wieacker-Wolff syndrome to the DNA, segment DXYS1 in proximal Xq. Am J Hum Genet 28:245-253
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.