FnuD II RFLP at the human dopamine-beta-hydroxylase (D beta H) locus.
作者信息
Perry S E, Phillips J A, Robertson D
机构信息
Department of Medicine, Vanderbilt University, Nashville, TN 37232.
出版信息
Nucleic Acids Res. 1991 Mar 11;19(5):1162. doi: 10.1093/nar/19.5.1162-a.
Abstract
摘要
相似文献
1
FnuD II RFLP at the human dopamine-beta-hydroxylase (D beta H) locus.人类多巴胺β-羟化酶（DβH）基因座处的FnuD II限制性片段长度多态性
Nucleic Acids Res. 1991 Mar 11;19(5):1162. doi: 10.1093/nar/19.5.1162-a.
2
Sequence tagged site (STS) TaqI RFLP at dopamine beta-hydroxylase (DBH).多巴胺β-羟化酶（DBH）处的序列标签位点（STS）TaqI限制性片段长度多态性
Nucleic Acids Res. 1991 Apr 25;19(8):1957. doi: 10.1093/nar/19.8.1957.
3
Linkage analysis of the human dopamine beta-hydroxylase gene.人类多巴胺β-羟化酶基因的连锁分析
Genomics. 1991 Jun;10(2):493-5. doi: 10.1016/0888-7543(91)90339-g.
4
RFLP for human DBH (dopamine beta-hydroxylase).人类多巴胺β-羟化酶（DBH）的限制性片段长度多态性分析
Nucleic Acids Res. 1990 Jan 25;18(2):387.
5
Two TaqI dimorphic sites at the human beta-hydroxylase locus.人类β-羟化酶基因座上的两个TaqI双态位点。
Nucleic Acids Res. 1989 Jul 25;17(14):5871. doi: 10.1093/nar/17.14.5871.
6
NcoI RFLP in the pseudogene (CYP2D8P) of the human debrisoquine 4-hydroxylase locus.人异喹胍4-羟化酶基因座假基因（CYP2D8P）中的NcoI限制性片段长度多态性
Nucleic Acids Res. 1991 Mar 11;19(5):1162. doi: 10.1093/nar/19.5.1162.
7
Dinucleotide repeat polymorphism at the human dopamine beta-hydroxylase (DBH) locus.人类多巴胺β-羟化酶（DBH）基因座的二核苷酸重复多态性。
Nucleic Acids Res. 1992 Mar 25;20(6):1429. doi: 10.1093/nar/20.6.1429.
8
PCR amplification of the Taq I B1/B2 polymorphism at intron 5 of the dopamine beta-hydroxylase gene.多巴胺β-羟化酶基因内含子5处Taq I B1/B2多态性的聚合酶链反应扩增
Psychiatr Genet. 1997 Spring;7(1):39-40. doi: 10.1097/00041444-199700710-00006.
9
PCR detection of the frequent TaqI RFLP at locus D21S13E.在D21S13E位点对常见的TaqI限制性片段长度多态性进行聚合酶链反应检测。
Nucleic Acids Res. 1991 May 11;19(9):2516. doi: 10.1093/nar/19.9.2516-a.
10
Detection of the XmnI RFLP at the human PAH locus by PCR.通过聚合酶链反应检测人类苯丙氨酸羟化酶基因座处的XmnI限制性片段长度多态性。
Nucleic Acids Res. 1992 Feb 25;20(4):927. doi: 10.1093/nar/20.4.927-a.
引用本文的文献
1
Dopamine beta-hydroxylase gene excluded in four subtypes of hereditary dystonia.
Hum Genet. 1991 Jul;87(3):311-6. doi: 10.1007/BF00200910.
2
Autonomic dysfunction: diagnosis guided by therapy.自主神经功能障碍：以治疗为导向的诊断
Trans Am Clin Climatol Assoc. 1992;103:228-37.
本文引用的文献
1
Human dopamine beta-hydroxylase gene: two mRNA types having different 3'-terminal regions are produced through alternative polyadenylation.人类多巴胺β-羟化酶基因：通过可变聚腺苷酸化产生具有不同3'末端区域的两种mRNA类型。
Nucleic Acids Res. 1989 Feb 11;17(3):1089-102. doi: 10.1093/nar/17.3.1089.
Zotero 插件