RFLPs for PstI and EcoRI in the human blood clotting factor X gene.
作者信息
Hay C W, Robertson K A, Fung M R, MacGillivray R T
出版信息
Nucleic Acids Res. 1986 Jun 25;14(12):5118. doi: 10.1093/nar/14.12.5118.
Abstract
摘要
相似文献
1
RFLPs for PstI and EcoRI in the human blood clotting factor X gene.人类凝血因子X基因中PstI和EcoRI的限制性片段长度多态性
Nucleic Acids Res. 1986 Jun 25;14(12):5118. doi: 10.1093/nar/14.12.5118.
2
Four RFLPs of the human insulin receptor gene: PstI, KpnI, RsaI (2 RFLPs).人类胰岛素受体基因的四种限制性片段长度多态性：PstI、KpnI、RsaI（两种限制性片段长度多态性）
Nucleic Acids Res. 1988 Aug 25;16(16):8204. doi: 10.1093/nar/16.16.8204.
3
Two EcoT14I RFLPs at the human renin (REN) gene locus.人类肾素（REN）基因位点的两个EcoT14I限制性片段长度多态性
Nucleic Acids Res. 1988 Jul 11;16(13):6253. doi: 10.1093/nar/16.13.6253.
4
Polymorphism associated with the human coagulation factor X (F10) gene.与人类凝血因子X（F10）基因相关的多态性。
Nucleic Acids Res. 1985 Nov 25;13(22):8286. doi: 10.1093/nar/13.22.8286.
5
Three RFLPs for the insulin receptor gene INSR: EcoRI, Pst I, Hind III.胰岛素受体基因INSR的三种限制性片段长度多态性：EcoRI、Pst I、Hind III。
Nucleic Acids Res. 1986 Aug 26;14(16):6776. doi: 10.1093/nar/14.16.6776.
6
Mucin 4 (MUC4) gene: regional assignment (3q29) and RFLP analysis.粘蛋白4（MUC4）基因：区域定位（3q29）及限制性片段长度多态性分析
Ann Genet. 1992;35(1):21-6.
7
Four RFLPs of the human insulin receptor gene: PstI, KpnI, RsaI (2 RFLPs).人类胰岛素受体基因的四种限制性片段长度多态性：PstI、KpnI、RsaI（两种限制性片段长度多态性）
Nucleic Acids Res. 1989 Jan 25;17(2):820. doi: 10.1093/nar/17.2.820.
8
The anonymous PAS45 probe detects RFLPs in 13q31.匿名的PAS45探针可检测13q31区域的限制性片段长度多态性（RFLP）。
Ann Genet. 1989;32(2):73-7.
9
Characterization of an almost full-length cDNA coding for human blood coagulation factor X.编码人凝血因子X的一个几乎全长的cDNA的特性分析
Proc Natl Acad Sci U S A. 1985 Jun;82(11):3591-5. doi: 10.1073/pnas.82.11.3591.
10
The gene for clotting factor 10 is mapped to 13q32----qter.
Cytogenet Cell Genet. 1986;41(3):185-8. doi: 10.1159/000132225.
引用本文的文献
1
Molecular genetic analysis of factor X deficiency: gene deletion and germline mosaicism.
Hum Genet. 1991 Jan;86(3):273-8. doi: 10.1007/BF00202408.
本文引用的文献
1
The structural gene for human coagulation factor X is located on chromosome 13q34.
Cytogenet Cell Genet. 1985;39(3):231-3. doi: 10.1159/000132141.
2
Characterization of an almost full-length cDNA coding for human blood coagulation factor X.编码人凝血因子X的一个几乎全长的cDNA的特性分析
Proc Natl Acad Sci U S A. 1985 Jun;82(11):3591-5. doi: 10.1073/pnas.82.11.3591.
Zotero 插件