Significantly higher frequency of the MspI 2.2 kb allele of the Duchenne muscular dystrophy intragenic probe P-20 in the Chinese population

Jianjun Wei; Yishou Guo; Bingxi Chen; Yaping Yang

doi:10.1007/BF00210761

Significantly higher frequency of the MspI 2.2 kb allele of the Duchenne muscular dystrophy intragenic probe P-20 in the Chinese population

Jianjun Wei^*, Yishou Guo, Bingxi Chen, Yaping Yang

^*Corresponding author for this work

Pathology

Research output: Contribution to journal › Article › peer-review

Abstract

The P-20 intragenic marker was used to test for restriction fragment length polymorphisms in unrelated Chinese patients with Duchenne or Becker muscular dystrophy or X-linked mental retardation. In addition to polymorphism at the 6.0/3.5kb MspI allelic site, we found an independent and high frequency of polymorphism at the 2.2/1.8kb site. This differs from results found with other populations.

Original language	English (US)
Pages (from-to)	149-150
Number of pages	2
Journal	Human Genetics
Volume	90
Issue number	1-2
DOIs	https://doi.org/10.1007/BF00210761
State	Published - Sep 1 1992

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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10.1007/BF00210761

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title = "Significantly higher frequency of the MspI 2.2 kb allele of the Duchenne muscular dystrophy intragenic probe P-20 in the Chinese population",

abstract = "The P-20 intragenic marker was used to test for restriction fragment length polymorphisms in unrelated Chinese patients with Duchenne or Becker muscular dystrophy or X-linked mental retardation. In addition to polymorphism at the 6.0/3.5kb MspI allelic site, we found an independent and high frequency of polymorphism at the 2.2/1.8kb site. This differs from results found with other populations.",

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AU - Wei, Jianjun

AU - Guo, Yishou

AU - Chen, Bingxi

AU - Yang, Yaping

PY - 1992/9/1

Y1 - 1992/9/1

N2 - The P-20 intragenic marker was used to test for restriction fragment length polymorphisms in unrelated Chinese patients with Duchenne or Becker muscular dystrophy or X-linked mental retardation. In addition to polymorphism at the 6.0/3.5kb MspI allelic site, we found an independent and high frequency of polymorphism at the 2.2/1.8kb site. This differs from results found with other populations.

AB - The P-20 intragenic marker was used to test for restriction fragment length polymorphisms in unrelated Chinese patients with Duchenne or Becker muscular dystrophy or X-linked mental retardation. In addition to polymorphism at the 6.0/3.5kb MspI allelic site, we found an independent and high frequency of polymorphism at the 2.2/1.8kb site. This differs from results found with other populations.

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ER -

Significantly higher frequency of the MspI 2.2 kb allele of the Duchenne muscular dystrophy intragenic probe P-20 in the Chinese population

Abstract

ASJC Scopus subject areas

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