메뉴 건너뛰기




Volumn 60, Issue 6, 1997, Pages 1468-1473

Localization of a novel X-linked progressive cone dystrophy gene to Xq27: Evidence for genetic heterogeneity

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

EID: 0030922081     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/515458     Document Type: Article
Times cited : (36)

References (19)
  • 1
    • 0000914411 scopus 로고
    • Cone dystrophy (X-linked) (COD1) maps between DXS7 (L1.28) and DXS206 (XJ1.1) and is linked to DXS84 (754)
    • Bartley J, Gies C, Jacobson D (1989) Cone dystrophy (X-linked) (COD1) maps between DXS7 (L1.28) and DXS206 (XJ1.1) and is linked to DXS84 (754). Cytogenet Cell Genet 51:959
    • (1989) Cytogenet Cell Genet , vol.51 , pp. 959
    • Bartley, J.1    Gies, C.2    Jacobson, D.3
  • 2
  • 4
    • 0027399171 scopus 로고
    • Detection of a new submicroscopic Norrie disease deletion interval with a novel DNA probe isolated by differential ALU PCR fingerprint cloning
    • Bergen AAB, Wapenaar MC, Schuurman EJM, Diergaarde PJ, Lerach H, Monaco AP, Bakker E, et al (1993b) Detection of a new submicroscopic Norrie disease deletion interval with a novel DNA probe isolated by differential ALU PCR fingerprint cloning. Cytogenet Cell Genet 624:231-235
    • (1993) Cytogenet Cell Genet , vol.624 , pp. 231-235
    • Bergen, A.A.B.1    Wapenaar, M.C.2    Schuurman, E.J.M.3    Diergaarde, P.J.4    Lerach, H.5    Monaco, A.P.6    Bakker, E.7
  • 5
    • 0019436216 scopus 로고
    • Congenital X-linked incomplete achromatopsia: Evidence for slow progression, carrier fundus findings, and possible genetic linkage with the G6PD locus
    • Fleischman JA, O'Donnell FE (1981) Congenital X-linked incomplete achromatopsia: evidence for slow progression, carrier fundus findings, and possible genetic linkage with the G6PD locus. Arch Ophthalmol 99:468-472
    • (1981) Arch Ophthalmol , vol.99 , pp. 468-472
    • Fleischman, J.A.1    O'Donnell, F.E.2
  • 6
    • 16944364197 scopus 로고
    • X-linked recessive cone dystrophy with a tapetal-like sheen
    • Heckenlively JR, Weleber RG (1986) X-linked recessive cone dystrophy with a tapetal-like sheen. Arch Ophthalmol 104: 324-328
    • (1986) Arch Ophthalmol , vol.104 , pp. 324-328
    • Heckenlively, J.R.1    Weleber, R.G.2
  • 7
    • 0028126874 scopus 로고
    • Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1)
    • Hong H-K, Ferrell RE, Gorin MB (1994) Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1). Am J Hum Genet 55:1173-1181
    • (1994) Am J Hum Genet , vol.55 , pp. 1173-1181
    • Hong, H.-K.1    Ferrell, R.E.2    Gorin, M.B.3
  • 8
    • 16944364053 scopus 로고
    • Localization of an X-linked progressive cone degeneration to Xp11 region. 8th International Congress of Human Genetics
    • Hong H-K, Ferrell RE, Paul TO, Gorin MB (1991) Localization of an X-linked progressive cone degeneration to Xp11 region. 8th International Congress of Human Genetics. Am J Hum Genet Suppl 49:138
    • (1991) Am J Hum Genet Suppl , vol.49 , pp. 138
    • Hong, H.-K.1    Ferrell, R.E.2    Paul, T.O.3    Gorin, M.B.4
  • 10
    • 0025605483 scopus 로고
    • Color matching and foveal densiometry in patients and carriers of an X-linked progressive cone dystrophy
    • Keunen JE, van Everdingen JA, Went LN, Oosterhuis JA, Norren van D (1990) Color matching and foveal densiometry in patients and carriers of an X-linked progressive cone dystrophy. Arch Ophthalmol 108:1713-1719
    • (1990) Arch Ophthalmol , vol.108 , pp. 1713-1719
    • Keunen, J.E.1    Van Everdingen, J.A.2    Went, L.N.3    Oosterhuis, J.A.4    Van Norren, D.5
  • 11
    • 0027979863 scopus 로고
    • X-linked progressive cone dystrophy: Localization of the gene locus to Xp21.1-p11.1 by linkage analysis
    • Meire FM, Bergen AAB, de Rouck A, Leys M, Delleman JW (1994) X-linked progressive cone dystrophy: localization of the gene locus to Xp21.1-p11.1 by linkage analysis. Br J Ophthalmol 78:103-108
    • (1994) Br J Ophthalmol , vol.78 , pp. 103-108
    • Meire, F.M.1    Bergen, A.A.B.2    De Rouck, A.3    Leys, M.4    Delleman, J.W.5
  • 13
    • 0026726294 scopus 로고
    • Berson test for blue cone monochromatism
    • Pinckers AJLG (1992) Berson test for blue cone monochromatism. Int Ophthalmol 16:185-186
    • (1992) Int Ophthalmol , vol.16 , pp. 185-186
    • Pinckers, A.J.L.G.1
  • 14
    • 0023219536 scopus 로고
    • X-linked cone dystrophy: An overlooked diagnosis?
    • Pinckers AJLG, Deutman AF (1987) X-linked cone dystrophy: an overlooked diagnosis? Int Ophthalmol 10:241-243
    • (1987) Int Ophthalmol , vol.10 , pp. 241-243
    • Pinckers, A.J.L.G.1    Deutman, A.F.2
  • 17
    • 0024454013 scopus 로고
    • An electroretinographic and molecular genetic study of X-linked cone degeneration
    • Reichel E, Bruce AM, Sandberg MA, Berson EL (1989) An electroretinographic and molecular genetic study of X-linked cone degeneration. Am J Ophthalmol 108:540-547
    • (1989) Am J Ophthalmol , vol.108 , pp. 540-547
    • Reichel, E.1    Bruce, A.M.2    Sandberg, M.A.3    Berson, E.L.4
  • 18


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.