메뉴 건너뛰기




Volumn 34, Issue 12, 1997, Pages 961-966

An ancestral core haplotype defines the critical region harbouring the North Carolina macular dystrophy gene (MCDR1)

Author keywords

CAPED; Chromosome 6q14 q16.2; Linkage analysis; NCMD

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BREAST AREOLA; CHROMOSOME 6Q; CLINICAL ARTICLE; FAMILIAL DISEASE; FEMALE; GENE MAPPING; HAPLOTYPE; HUMAN; MALE; MOLECULAR CLONING; PIGMENT EPITHELIUM; PRIORITY JOURNAL; RETINA MACULA DEGENERATION; UNITED STATES;

EID: 0030774056     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.34.12.961     Document Type: Article
Times cited : (23)

References (18)
  • 4
    • 0021194060 scopus 로고
    • Central areolar pigment epithelial dystrophy
    • Hermsen VM, Judisch GF. Central areolar pigment epithelial dystrophy. Ophthalmologica 1984;189:69-72.
    • (1984) Ophthalmologica , vol.189 , pp. 69-72
    • Hermsen, V.M.1    Judisch, G.F.2
  • 5
    • 0026594081 scopus 로고
    • North Carolina macular dystrophy and central areolar pigment epithelial dystrophy: One family, one disease
    • Small KW, Hermsen V, Gurney N, Fetkenhour CL, Folk JC. North Carolina macular dystrophy and central areolar pigment epithelial dystrophy: one family, one disease. Arch Ophthalmol 1992;110:515-18.
    • (1992) Arch Ophthalmol , vol.110 , pp. 515-518
    • Small, K.W.1    Hermsen, V.2    Gurney, N.3    Fetkenhour, C.L.4    Folk, J.C.5
  • 6
    • 0031546130 scopus 로고    scopus 로고
    • North Carolina macular dystrophy phenotype in France maps to the MCDR1 locus
    • Small KW, Puech B, Mullen L, Yelchits S. North Carolina macular dystrophy phenotype in France maps to the MCDR1 locus. Mol Vis 1997;3:1-6.
    • (1997) Mol Vis , vol.3 , pp. 1-6
    • Small, K.W.1    Puech, B.2    Mullen, L.3    Yelchits, S.4
  • 7
    • 84907113514 scopus 로고
    • North Carolina macular dystrophy (MCDR1). A review and refined mapping to 6q14-q12.2
    • Small KW, Weber JL, Roses A, Pericak-Vance MA. North Carolina macular dystrophy (MCDR1). A review and refined mapping to 6q14-q12.2. Ophthal Paediatr Genet 1993;14:143-50.
    • (1993) Ophthal Paediatr Genet , vol.14 , pp. 143-150
    • Small, K.W.1    Weber, J.L.2    Roses, A.3    Pericak-Vance, M.A.4
  • 8
    • 0028946003 scopus 로고
    • Autosomal dominant macular dystrophy simulating North Carolina macular dystrophy
    • Holz FG, Evans K, Gregory CY, Bhattacharya S, Bird AC. Autosomal dominant macular dystrophy simulating North Carolina macular dystrophy. Arch Ophthalmol 1995;113:178-84.
    • (1995) Arch Ophthalmol , vol.113 , pp. 178-184
    • Holz, F.G.1    Evans, K.2    Gregory, C.Y.3    Bhattacharya, S.4    Bird, A.C.5
  • 9
    • 0029127270 scopus 로고
    • Localization of the gene for progressive bifocal chorioretinal atrophy (PBCRA) to chromosome 6q
    • Kelsell RE, Godley BE, Evans K, et al. Localization of the gene for progressive bifocal chorioretinal atrophy (PBCRA) to chromosome 6q. Hum Mol Genet 1995;4:1653-6.
    • (1995) Hum Mol Genet , vol.4 , pp. 1653-1656
    • Kelsell, R.E.1    Godley, B.E.2    Evans, K.3
  • 10
    • 0024423668 scopus 로고
    • Identification of the cystic fibrosis gene: Genetic analysis
    • Kerem BS, Rommens JM, Buchanan JA, et al. Identification of the cystic fibrosis gene: genetic analysis. Science 1989;245:1073-80.
    • (1989) Science , vol.245 , pp. 1073-1080
    • Kerem, B.S.1    Rommens, J.M.2    Buchanan, J.A.3
  • 11
    • 0024456037 scopus 로고
    • Non-random association between alleles detected at D4S95 and D4S98 and the Huntington's disease gene
    • Theilmann J, Kanani S, Shiang R, et al. Non-random association between alleles detected at D4S95 and D4S98 and the Huntington's disease gene. J Med Genet 1989;26:676-81.
    • (1989) J Med Genet , vol.26 , pp. 676-681
    • Theilmann, J.1    Kanani, S.2    Shiang, R.3
  • 12
    • 0025912905 scopus 로고
    • Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker
    • Harley HG, Brook JD, Floyd J, et al. Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker. Am J Hum Genet 1991;49:68-75.
    • (1991) Am J Hum Genet , vol.49 , pp. 68-75
    • Harley, H.G.1    Brook, J.D.2    Floyd, J.3
  • 13
    • 0026814864 scopus 로고
    • Die zentrale areoläre Pigmentepitheldystrophie
    • Käsmann B, Blankenagel A, Daus W. Die zentrale areoläre Pigmentepitheldystrophie. Ophthalmologe 1992;89:60-6.
    • (1992) Ophthalmologe , vol.89 , pp. 60-66
    • Käsmann, B.1    Blankenagel, A.2    Daus, W.3
  • 14
    • 0024853502 scopus 로고
    • North Carolina macular dystrophy revisited
    • Small KW. North Carolina macular dystrophy revisited. Ophthalmology 1989;96:1747-54.
    • (1989) Ophthalmology , vol.96 , pp. 1747-1754
    • Small, K.W.1
  • 15
    • 1842353216 scopus 로고
    • Analysis of human Y chromosome specific reiterated DNA in chromosome variants
    • Kunkel LM, Smith KD, Boyer SH, et al. Analysis of human Y chromosome specific reiterated DNA in chromosome variants. Proc Natl Acad Sci USA 1977;74:1245-9.
    • (1977) Proc Natl Acad Sci USA , vol.74 , pp. 1245-1249
    • Kunkel, L.M.1    Smith, K.D.2    Boyer, S.H.3
  • 16
    • 0021850103 scopus 로고
    • Multilocus linkage analysis in humans: Detection of linkage and estimation of recombination
    • Lathrop GM, Lalouel JM, Julier C, Ott J. Multilocus linkage analysis in humans: detection of linkage and estimation of recombination. Am J Hum Genet 1985;37:482-98.
    • (1985) Am J Hum Genet , vol.37 , pp. 482-498
    • Lathrop, G.M.1    Lalouel, J.M.2    Julier, C.3    Ott, J.4
  • 17
    • 0000951097 scopus 로고
    • The evolutionary dynamics of complex polymorphisms
    • Lewontin RC, Kojima KI. The evolutionary dynamics of complex polymorphisms. Evolution 1960;14:458-72.
    • (1960) Evolution , vol.14 , pp. 458-472
    • Lewontin, R.C.1    Kojima, K.I.2
  • 18
    • 0007758208 scopus 로고
    • Polymorphism of DNA sequence adjacent to human beta globin structural gene: Relationship to sickle mutation
    • Kan YW, Dozy AM. Polymorphism of DNA sequence adjacent to human beta globin structural gene: relationship to sickle mutation. Proc Natl Acad Sci USA 1978;78:5631-5.
    • (1978) Proc Natl Acad Sci USA , vol.78 , pp. 5631-5635
    • Kan, Y.W.1    Dozy, A.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.