1994
DOI: 10.1006/geno.1994.1280
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Assignment of 112 Microsatellite Markers to 23 Chromosome 11 Subregions Delineated by Somatic Hybrids: Comparison with the Genetic Map

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Cited by 23 publications
(13 citation statements)
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“…The marker HBB (HinfI polymorphism) (Semenza et al, 1989) is positioned at 170 kb, D11S1758 (dinucleotide polymorphism) (Couillin et al, 1994) is positioned between 410 and 480 kb, D11S988 (dinucleotide polymorphism) (primers 1019/1020, GenBank Accession No. L20023) is positioned between 635 and 685 kb, D11S12 (MspI polymorphism) (Barker et al, 1984) is positioned at 1025 kb, RRM1 (SacI polymorphism) (Byrne and Smith, 1990) is positioned at 1090 kb, and D11S860 (dinucleotide polymorphism) (McNoe et al, 1992) is positioned between 1265 and 1290 kb.…”
Section: Position and Distances Of Polymorphic Markersmentioning
confidence: 99%
“…The marker HBB (HinfI polymorphism) (Semenza et al, 1989) is positioned at 170 kb, D11S1758 (dinucleotide polymorphism) (Couillin et al, 1994) is positioned between 410 and 480 kb, D11S988 (dinucleotide polymorphism) (primers 1019/1020, GenBank Accession No. L20023) is positioned between 635 and 685 kb, D11S12 (MspI polymorphism) (Barker et al, 1984) is positioned at 1025 kb, RRM1 (SacI polymorphism) (Byrne and Smith, 1990) is positioned at 1090 kb, and D11S860 (dinucleotide polymorphism) (McNoe et al, 1992) is positioned between 1265 and 1290 kb.…”
Section: Position and Distances Of Polymorphic Markersmentioning
confidence: 99%
“…Oligonucleotide primer pairs for four microsatellite regions containing (CA)n dinucleotide repeat (D11S935, D11S905, D11S934, D11S912) [23] were synthesized on a DNA synthesizer (Applied Biosystems, Foster City, CA, USA). The oligonucleotide primer was end-labeled with [r-32 P]adenosine 5Ј-triphosphates (Amersham, Tokyo, Japan) at 3,000 Ci/mmol using T4 polynucleotide kinase (New England Biolabs, Beverly, MA, USA), followed by the removal of unincorporated 32 P by using a spin column.…”
Section: Pcr Parametersmentioning
confidence: 99%
“…Positional cloning of disease loci can benefit from a variety of 11p15 maps. A large number of new polymorphic markers have recently been identified (Takiia et al, 1992;Weissenbach et al, 1992;Couillin et al} 1994), which will facilitate the construction of a high-resolution genetic map (O'Rahilly et al, 1992;NIHlCEPH Collaborative Mapping Group, 1992;Litt et al, 1993;Gyapay et al, 1994). Large numbers of other probes have been generated and mapped within 11p15, and ordered clone maps are under way (GIaser et al, 1989;Harrison-Lavoie et al, 1989;Newsham et al, 1991;Heding et al, 1992;Puech et al, 1992).…”
mentioning
confidence: 99%