Partitioned pulsed-field gel electrophoresis-PCR (PPF-PCR): a new method for pulsed-field mapping for STS and microsatellites.
作者信息
Denton P H, Cullen J B, Loeb D, Lucas A, Nunes K, Hulett C, Vance J M
机构信息
Division of Neurology, Duke University Medical Center, Durham, NC.
出版信息
Nucleic Acids Res. 1994 May 11;22(9):1776-7. doi: 10.1093/nar/22.9.1776.
Abstract
摘要
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本文引用的文献
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Interspersed repetitive sequence (IRS)-PCR amplification of pulsed-field gel fractionated DNA to derive markers from the incontinentia pigmenti 1 (IP1) locus.对脉冲场凝胶分级分离的DNA进行散布重复序列（IRS）-PCR扩增，以从色素失禁1（IP1）基因座获得标记。
Nucleic Acids Res. 1993 Jan 11;21(1):175-6. doi: 10.1093/nar/21.1.175.
2
Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q.常染色体隐性遗传性夏科-马里-图斯病的一个基因座（CMT4A）与8号染色体长臂的连锁关系。
Hum Mol Genet. 1993 Oct;2(10):1625-8. doi: 10.1093/hmg/2.10.1625.
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Dinucleotide repeat polymorphism at the D15S87 locus.D15S87基因座的二核苷酸重复多态性
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A genetic map of human chromosome 17p.
Genomics. 1990 May;7(1):103-9. doi: 10.1016/0888-7543(90)90524-x.
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Human-specific amplification of radiation hybrid DNA fractionated by pulsed-field gel electrophoresis.通过脉冲场凝胶电泳分离的辐射杂种DNA的人类特异性扩增。
Nucleic Acids Res. 1991 Jan 25;19(2):401-2. doi: 10.1093/nar/19.2.401.
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Charcot-Marie-Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unit.1A型遗传性运动感觉神经病的重复现象似乎源于1.5 Mb单体单元侧翼重复序列处的重组。
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