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0028851065
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Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15
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The gene for Best's macular dystrophy is located at 11q13 in a Swedish family
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Forsman K, Graff C, Nordström S, Johansson K, Westermark E, Lundgren E, Gustavson K-H, Wadelius C, Holmgren G. The gene for Best's macular dystrophy is located at 11q13 in a Swedish family. Clin Genet 1992: 42: 156-159.
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0028603301
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Fine mapping of Best's macular dystrophy localises the gene in close proximity to but distinct from the D11S480/ROM1 loci
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Graff C, Forsman K, Larsson C, Nordström S, Lind L, Johansson L, Sandgren O, Weissenbach J, Holmgren G, Gustavson K-H, Wadelius C, Fine mapping of Best's macular dystrophy localises the gene in close proximity to but distinct from the D11S480/ROM1 loci. Genomics 1994: 24: 425-434.
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Hereditary macular degeneration (HMD) in 246 cases traced to one gene-source in central Sweden
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Determination of allele frequencies at loci with length polymorphism by quantitative analysis of DNA amplified from pooled samples
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A manifold support for molecular genetic reactions
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Parik J, Kwiatkowski M, Lagerkvist A, Lagerstrom Fermer M, Samiotaki M, Stewart J, Glad G, Mendel-Hartvig M, Landegren U. A manifold support for molecular genetic reactions. Anal Biochem 1993: 211: 144-150.
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Toward fully automated genotyping: Genotyping microsatellite markers by deconvolution
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13
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0028000502
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Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping
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Sheffield VC, Carmi R, Kwitek-Black A, Rokhlina T, Nishimura D, Duyk GM, Elbedour K, Sunden SL, Stone EM. Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping. Hum Mol Genet 1994: 3: 1331-1335.
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15
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0028837439
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A recombination event excludes the ROM1 Jocus from the Best's vitelliform macular dystrophy region
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Stöhr H, Weber BH. A recombination event excludes the ROM1 Jocus from the Best's vitelliform macular dystrophy region. Hum Genet 1995: 95: 219-222.
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Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13
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Stone EM, Nichols BE, Streb LM, Kimura AE, Sheffield VC. Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13. Nat Genet 1992: 1: 246-250.
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17
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0029128302
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A gene causing Hermansky-Pudlak syndrome in a Puerto Rican population maps to chromosome 10q2
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Wildenberg SC, Getting WS, Almodo'var C, Krumwiede M, White JG, King RA. A gene causing Hermansky-Pudlak syndrome in a Puerto Rican population maps to chromosome 10q2. Am J Hum Genet 1995: 57: 755-765.
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