A rare TaqI RFLP immediately 3' of the HEXB gene on chromosome 5.
作者信息
Wood S, Schertzer M, Neote K
机构信息
Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
出版信息
Nucleic Acids Res. 1989 Mar 25;17(6):2368. doi: 10.1093/nar/17.6.2368.
Abstract
摘要
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A rare TaqI RFLP immediately 3' of the HEXB gene on chromosome 5.位于5号染色体上HEXB基因3'端紧邻处的一种罕见的TaqI限制性片段长度多态性。
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A TaqI RFLP at the DRD1 locus.DRD1基因座处的TaqI限制性片段长度多态性
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XmnI RFLP at 5q13 detected by a 0.49 kb Xmn I fragment of human hexosaminidase (HEXB) cDNA.通过人己糖胺酶（HEXB）cDNA的0.49 kb XmnI片段检测到5q13处的XmnI限制性片段长度多态性。
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An arbitrary single copy sequence VC64 [D1S86] detects a moderate frequency TaqI RFLP on chromosome 1.任意一个单拷贝序列VC64 [D1S86]在1号染色体上检测到中等频率的TaqI限制性片段长度多态性。
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TaqI RFLP at 19q13.1 identified by the anonymous DNA sequence p5B18 [D19S28].由匿名DNA序列p5B18 [D19S28]鉴定的19q13.1处的TaqI限制性片段长度多态性
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A high frequency two allele TaqI RFLP detected by an anonymous sequence VC61 [D2S65] on chromosome 2.通过2号染色体上一个名为VC61 [D2S65]的匿名序列检测到的高频双等位基因TaqI限制性片段长度多态性。
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A high frequency two allele TaqI RFLP detected by an anonymous sequence VC61 [D2S65] on chromosome 2.通过位于2号染色体上的一个无名序列VC61 [D2S65]检测到的高频双等位基因TaqI限制性片段长度多态性。
Nucleic Acids Res. 1989 Jul 11;17(13):5424. doi: 10.1093/nar/17.13.5424.
本文引用的文献
1
Selective linkage disruption in human-Chinese hamster cell hybrids: deletion mapping of the leuS, hexB, emtB, and chr genes on human chromosome 5.人-中国仓鼠细胞杂种中的选择性连锁破坏：人类5号染色体上leuS、hexB、emtB和chr基因的缺失定位
Mol Cell Biol. 1982 Oct;2(10):1220-8. doi: 10.1128/mcb.2.10.1220-1228.1982.
2
Characterization of the human HEXB gene encoding lysosomal beta-hexosaminidase.
Genomics. 1988 Nov;3(4):279-86. doi: 10.1016/0888-7543(88)90116-4.
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