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A polymorphic human myosin heavy chain locus is linked to an anonymous single copy locus (D17S1) at 17p13.

作者信息

Schwartz C E, McNally E, Leinwand L, Skolnick M H

出版信息

Cytogenet Cell Genet. 1986;43(1-2):117-20. doi: 10.1159/000132307.

DOI:10.1159/000132307
PMID:2877813
Abstract

Restriction fragment length polymorphisms (RFLPs) have been developed for an adult human skeletal muscle myosin heavy chain gene which was previously mapped to the short arm of human chromosome 17. Using RFLP analysis of DNA from 140 individuals, we have found tight linkage (LOD score of 6.9) between this myosin heavy chain gene and the anonymous DNA probe, D17S1.

摘要

相似文献

1
A polymorphic human myosin heavy chain locus is linked to an anonymous single copy locus (D17S1) at 17p13.
Cytogenet Cell Genet. 1986;43(1-2):117-20. doi: 10.1159/000132307.
2
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引用本文的文献

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Arch fingerprints, hypotonia, and areflexia associated with X linked mental retardation.与X连锁智力迟钝相关的弓形指纹、肌张力减退和反射消失。
J Med Genet. 1997 Jun;34(6):465-9. doi: 10.1136/jmg.34.6.465.
3
Deletion (X)(q26.1-->q28) in a proband and her mother: molecular characterization and phenotypic-karyotypic deductions.
先证者及其母亲的X染色体缺失(X)(q26.1→q28):分子特征分析及表型-核型推断
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Two sisters with a distal deletion at the Xq26/Xq27 interface: DNA studies indicate that the gene locus for factor IX is present.两姐妹在Xq26/Xq27界面处存在远端缺失:DNA研究表明存在IX因子的基因座。
Hum Genet. 1987 May;76(1):54-7. doi: 10.1007/BF00283050.
5
Mapping of Alport syndrome to the long arm of the X chromosome.奥尔波特综合征基因定位到X染色体长臂
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The parental origin and mechanism of formation of three dicentric X chromosomes.三条双着丝粒X染色体的亲本来源及形成机制。
Hum Genet. 1988 Sep;80(1):81-4. doi: 10.1007/BF00451462.
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Detection of submicroscopic deletions in band 17p13 in patients with the Miller-Dieker syndrome.米勒-迪克尔综合征患者17p13带亚显微缺失的检测
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