메뉴 건너뛰기




Volumn 60, Issue 5, 1997, Pages 1139-1149

Linkage disequilibrium and physical mapping of X-linked juvenile retinoschisis

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; CONTROLLED STUDY; FEMALE; FINLAND; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENE MAPPING; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; PREVALENCE; PRIORITY JOURNAL; RECESSIVE INHERITANCE; RESTRICTION MAPPING; RETINOSCHISIS; SEQUENCE TAGGED SITE; VISUAL ACUITY; YEAST ARTIFICIAL CHROMOSOME;

EID: 0030955038     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (21)

References (53)
  • 1
    • 0025368589 scopus 로고
    • Construction and characterization of a yeast artificial chromosome library containing seven haploid human genome equivalents
    • Albertsen HM, Abderrahim H, Cann HM, Dausset J, Le Paslier D, Cohen D (1990) Construction and characterization of a yeast artificial chromosome library containing seven haploid human genome equivalents. Proc Natl Acad Sci USA 87:4256-4260
    • (1990) Proc Natl Acad Sci USA , vol.87 , pp. 4256-4260
    • Albertsen, H.M.1    Abderrahim, H.2    Cann, H.M.3    Dausset, J.4    Le Paslier, D.5    Cohen, D.6
  • 4
    • 0028942620 scopus 로고
    • A 6 Mb YAC contig in Xp22.1-Xp22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3 and PHKA2 genes
    • Alitalo T, Francis F, Kere J, Lehrach H, Schlessinger D, Willard HF (1995) A 6 Mb YAC contig in Xp22.1-Xp22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3 and PHKA2 genes. Genomics 25:691-700
    • (1995) Genomics , vol.25 , pp. 691-700
    • Alitalo, T.1    Francis, F.2    Kere, J.3    Lehrach, H.4    Schlessinger, D.5    Willard, H.F.6
  • 5
    • 0023200798 scopus 로고
    • X-linked retinoschisis is closely linked to DXS41 and DXS16 but not DXS85
    • Alitalo T, Kärnä J, Forsius H, de la Chapelle A (1987) X-linked retinoschisis is closely linked to DXS41 and DXS16 but not DXS85. Clin Genet 32:192-195
    • (1987) Clin Genet , vol.32 , pp. 192-195
    • Alitalo, T.1    Kärnä, J.2    Forsius, H.3    De La Chapelle, A.4
  • 6
    • 0026033654 scopus 로고
    • Refined localization of the gene causing X-linked juvenile retinoschisis
    • Alitalo T, Kruse TA, de la Chapelle A (1991) Refined localization of the gene causing X-linked juvenile retinoschisis. Genomics 9:505-510
    • (1991) Genomics , vol.9 , pp. 505-510
    • Alitalo, T.1    Kruse, T.A.2    De La Chapelle, A.3
  • 8
    • 0025835296 scopus 로고
    • Fast and sensitive silver staining of DNA in polyacrylamide gels
    • Bassam BJ, Caetano-Anolles G, Gresshoff PM (1991) Fast and sensitive silver staining of DNA in polyacrylamide gels. Anal Biochem 196:80-83
    • (1991) Anal Biochem , vol.196 , pp. 80-83
    • Bassam, B.J.1    Caetano-Anolles, G.2    Gresshoff, P.M.3
  • 10
    • 0024805395 scopus 로고
    • The isochore organization of the human genome
    • Bernardi G (1989) The isochore organization of the human genome. Annu Rev Genet 23:637-661
    • (1989) Annu Rev Genet , vol.23 , pp. 637-661
    • Bernardi, G.1
  • 11
    • 0026878925 scopus 로고
    • Dinucleotide repeat polymorphisms at the DXS365, DXS443 and DXS451 loci
    • Browne D, Barker D, Litt M (1992) Dinucleotide repeat polymorphisms at the DXS365, DXS443 and DXS451 loci. Hum Mol Genet 1:213
    • (1992) Hum Mol Genet , vol.1 , pp. 213
    • Browne, D.1    Barker, D.2    Litt, M.3
  • 12
    • 0022558970 scopus 로고
    • Congenital hereditary (juvenile X-linked) retinoschisis: Histopathologic and ultrastructural findings in three eyes
    • Condon GP, Brownstein S, Wang N-S, Kearns JAF, Ewing CC (1986) Congenital hereditary (juvenile X-linked) retinoschisis: histopathologic and ultrastructural findings in three eyes. Arch Ophthalmol 104:576-583
    • (1986) Arch Ophthalmol , vol.104 , pp. 576-583
    • Condon, G.P.1    Brownstein, S.2    Wang, N.-S.3    Kearns, J.A.F.4    Ewing, C.C.5
  • 15
    • 0027507885 scopus 로고
    • Disease gene mapping in isolated human populations: The example of Finland
    • de la Chapelle A (1993) Disease gene mapping in isolated human populations: the example of Finland. J Med Genet 30:857-865
    • (1993) J Med Genet , vol.30 , pp. 857-865
    • De La Chapelle, A.1
  • 17
    • 0029043706 scopus 로고
    • Genetic analysis of new French X-linked juvenile retinoschisis kindreds using microsatellite markers closely linked to the RS locus: Further narrowing of the RS candidate region
    • Dumur V, Trivier E, Puech B, Peugnet F, Zanlonghi X, Hache JC, Hanauer A (1995) Genetic analysis of new French X-linked juvenile retinoschisis kindreds using microsatellite markers closely linked to the RS locus: further narrowing of the RS candidate region. Hum Genet 96:79-82
    • (1995) Hum Genet , vol.96 , pp. 79-82
    • Dumur, V.1    Trivier, E.2    Puech, B.3    Peugnet, F.4    Zanlonghi, X.5    Hache, J.C.6    Hanauer, A.7
  • 21
    • 0023765785 scopus 로고
    • Linkage relationship between retinoschisis and four marker loci
    • Geliert G, Petersen J, Krawczak M, Zoll B (1988) Linkage relationship between retinoschisis and four marker loci. Hum Genet 79:382-384
    • (1988) Hum Genet , vol.79 , pp. 382-384
    • Geliert, G.1    Petersen, J.2    Krawczak, M.3    Zoll, B.4
  • 22
    • 0026949420 scopus 로고
    • Linkage disequilibrium mapping in isolated founder populations: Diastrophic dysplasia in Finland
    • Hästbacka J, de la Chapelle A, Kaitila I, Sistonen P, Weaver A, Lander E (1992) Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland. Nat Genet 2:204-211
    • (1992) Nat Genet , vol.2 , pp. 204-211
    • Hästbacka, J.1    De La Chapelle, A.2    Kaitila, I.3    Sistonen, P.4    Weaver, A.5    Lander, E.6
  • 23
    • 0027978110 scopus 로고
    • The diastrophic dysplasia gene encodes a novel sulfate transporter: Positional cloning by fine-structure linkage disequilibrium mapping
    • Hästbacka J, de la Chapelle A, Mahtani M, Clines G, Reeve-Daly MP, Daly M, Hamilton BA, et al (1994) The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping. Cell 78:1073-1087
    • (1994) Cell , vol.78 , pp. 1073-1087
    • Hästbacka, J.1    De La Chapelle, A.2    Mahtani, M.3    Clines, G.4    Reeve-Daly, M.P.5    Daly, M.6    Hamilton, B.A.7
  • 26
    • 0026440240 scopus 로고
    • Mapping human chromosomes by walking with sequence-tagged sites from end fragments of yeast artificial chromosome inserts
    • Kere J, Nagaraja R, Mumm S, Ciccodicola A, D'Urso M, Schlessinger D (1992) Mapping human chromosomes by walking with sequence-tagged sites from end fragments of yeast artificial chromosome inserts. Genomics 14:241-248
    • (1992) Genomics , vol.14 , pp. 241-248
    • Kere, J.1    Nagaraja, R.2    Mumm, S.3    Ciccodicola, A.4    D'Urso, M.5    Schlessinger, D.6
  • 28
    • 0025897085 scopus 로고
    • Yeast artificial chromosome libraries containing large inserts from mouse and human DNA
    • Larin Z, Monaco AP, Lehrach H (1991) Yeast artificial chromosome libraries containing large inserts from mouse and human DNA. Proc Natl Acad Sci USA 88:4123-4127
    • (1991) Proc Natl Acad Sci USA , vol.88 , pp. 4123-4127
    • Larin, Z.1    Monaco, A.P.2    Lehrach, H.3
  • 29
    • 0026742792 scopus 로고
    • CpG islands as gene markers in the human genome
    • Larsen F, Gundersen G, Lopez R, Prydz H (1992) CpG islands as gene markers in the human genome. Genomics 13:1095-1107
    • (1992) Genomics , vol.13 , pp. 1095-1107
    • Larsen, F.1    Gundersen, G.2    Lopez, R.3    Prydz, H.4
  • 31
    • 0027236091 scopus 로고
    • Localization of the EPM1 gene for progressive myoclonus epilepsy on chromosome 21: Linkage disequilibrium allows high resolution mapping
    • Lehesjoki A-E, Koskiniemi M, Norio R, Tirrito S, Sistonen P, Lander E, de la Chapelle A (1993) Localization of the EPM1 gene for progressive myoclonus epilepsy on chromosome 21: linkage disequilibrium allows high resolution mapping. Hum Mol Genet 2:1229-1234
    • (1993) Hum Mol Genet , vol.2 , pp. 1229-1234
    • Lehesjoki, A.-E.1    Koskiniemi, M.2    Norio, R.3    Tirrito, S.4    Sistonen, P.5    Lander, E.6    De La Chapelle, A.7
  • 34
    • 0028114080 scopus 로고
    • Characterization of four human YAC libraries for clone size, chimerism, and X chromosome sequence representation
    • Nagaraja R, Kere J, MacMillan S, Masisi W, Johnson D, Molini B, Wein K, et al (1994) Characterization of four human YAC libraries for clone size, chimerism, and X chromosome sequence representation. Nucleic Acids Res 22:3406-3411
    • (1994) Nucleic Acids Res , vol.22 , pp. 3406-3411
    • Nagaraja, R.1    Kere, J.2    MacMillan, S.3    Masisi, W.4    Johnson, D.5    Molini, B.6    Wein, K.7
  • 36
    • 0015436884 scopus 로고
    • The Finnish population structure: A genetic and genealogical study
    • Nevanlinna HR (1972) The Finnish population structure: a genetic and genealogical study. Hereditas 73:195-236
    • (1972) Hereditas , vol.73 , pp. 195-236
    • Nevanlinna, H.R.1
  • 37
    • 0002739198 scopus 로고
    • Diseases of Finland and Scandinavia
    • Rotchild H (ed) Academic Press, New York
    • Norio R (1981) Diseases of Finland and Scandinavia. In: Rotchild H (ed) Biocultural aspects of disease. Academic Press, New York, pp 359-415
    • (1981) Biocultural Aspects of Disease , pp. 359-415
    • Norio, R.1
  • 38
    • 0027415954 scopus 로고
    • Characterisation of a highly polymorphic microsatellite at the DXS257 locus: Confirmation of very close linkage to the retinoschisis disease gene
    • Oudet C, Weber C, Kaplan J, Segues B, Croquette M-F, Ollagnon Roman E, Hanauer A (1992) Characterisation of a highly polymorphic microsatellite at the DXS257 locus: confirmation of very close linkage to the retinoschisis disease gene. J Med Genet 30:300-303
    • (1992) J Med Genet , vol.30 , pp. 300-303
    • Oudet, C.1    Weber, C.2    Kaplan, J.3    Segues, B.4    Croquette, M.-F.5    Ollagnon Roman, E.6    Hanauer, A.7
  • 40
    • 16944367086 scopus 로고
    • Noormarkku
    • Öhling M, Lahtinen M, Osala T, Ahrner L (eds) ISBN 951-95005-6-1. Suomen Maakuntajulkaisu Oy, Vaasa, Finland
    • Peevo R (1977) Noormarkku. In: Öhling M, Lahtinen M, Osala T, Ahrner L (eds) Kotiseutuni. ISBN 951-95005-6-1. Suomen Maakuntajulkaisu Oy, Vaasa, Finland, pp 231-241
    • (1977) Kotiseutuni , pp. 231-241
    • Peevo, R.1
  • 42
    • 16944365121 scopus 로고
    • Kokemäki
    • Öhling M, Lahtinen M, Osala T, Ahrner L (ed) ISBN 951-95005-6-1. Suomen Maakuntajulkaisu Oy, Vaasa, Finland
    • Pertola E (1977) Kokemäki. In: Öhling M, Lahtinen M, Osala T, Ahrner L (ed) Kotiseutuni. ISBN 951-95005-6-1. Suomen Maakuntajulkaisu Oy, Vaasa, Finland, pp 170-178
    • (1977) Kotiseutuni , pp. 170-178
    • Pertola, E.1
  • 43
    • 0025816924 scopus 로고
    • Epidemiologie et prevalence des principales dystrophies rétiniennes héréditaires dans le Nord de la France
    • Puech B, Kostrubiec B, Hache J-C, Francois P (1991) Epidemiologie et prevalence des principales dystrophies rétiniennes héréditaires dans le Nord de la France. J Fr Ophtalmol 14: 153-164
    • (1991) J Fr Ophtalmol , vol.14 , pp. 153-164
    • Puech, B.1    Kostrubiec, B.2    Hache, J.-C.3    Francois, P.4
  • 47
    • 0028968329 scopus 로고
    • A powerful likelihood method for the analysis of linkage disequilibrium between trait loci and one or more polymorphic marker loci
    • Terwilliger JD (1995) A powerful likelihood method for the analysis of linkage disequilibrium between trait loci and one or more polymorphic marker loci. Am J Hum Genet 56: 777-787
    • (1995) Am J Hum Genet , vol.56 , pp. 777-787
    • Terwilliger, J.D.1
  • 53
    • 0020552956 scopus 로고
    • Linkage relationships between retinoschisis, Xg, and a cloned DNA sequence from the distal short arm of the X chromosome
    • Wieacker P, Wienker TF, Dallapiccola B, Bender K, Davies KE, Ropers HH (1983) Linkage relationships between retinoschisis, Xg, and a cloned DNA sequence from the distal short arm of the X chromosome. Hum Genet 64: 143-145
    • (1983) Hum Genet , vol.64 , pp. 143-145
    • Wieacker, P.1    Wienker, T.F.2    Dallapiccola, B.3    Bender, K.4    Davies, K.E.5    Ropers, H.H.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.