Evaluation of Microchip Electrophoresis as a Molecular Diagnostic Method for Duchenne Muscular Dystrophy-Reference-Cited by-同舟云学术

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Evaluation of Microchip Electrophoresis as a Molecular Diagnostic Method for Duchenne Muscular Dystrophy

Published:2002-02-01 Issue:2 Volume:48 Page:380-383
ISSN:0009-9147
Container-title:Clinical Chemistry
language:en
Short-container-title:

Author:

Ferrance Jerome¹,Snow Karen²,Landers James P¹³

Affiliation:

1. Department of Chemistry, McCormick Road, University of Virginia, Charlottesville, VA 22901

2. Molecular Genetics Laboratory, Mayo Clinic, Rochester, MN 55905

3. Department of Pathology, University of Virginia Health Science Center, Charlottesville, VA 22901

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

Link

http://academic.oup.com/clinchem/article-pdf/48/2/380/32733925/clinchem0380.pdf

Reference18 articles.

1. Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification

2. Diagnosis of Duchenne/Becker muscular dystrophy and quantitative identification of carrier status by use of entangled solution capillary electrophoresis

Cited by 13 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Miniaturization of molecular biological techniques for gene assay;The Analyst;2010

2. CE-based detection of methicillin-resistantStaphylococcus aureus;ELECTROPHORESIS;2009-02

3. DNA Diagnostics by Capillary Electrophoresis;Chemical Reviews;2007-10-31

4. Clinical Analysis by Microchip Capillary Electrophoresis;Clinical Chemistry;2006-01-01

5. Denaturing HPLC Coupled with Multiplex PCR for Rapid Detection of Large Deletions in Duchenne Muscular Dystrophy Carriers;Clinical Chemistry;2005-07-01

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