Comparative analysis of PCR-deletion detection and immunohistochemistry in Brazilian Duchenne and Becker muscular dystrophy patients
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference53 articles.
1. A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methods.
2. Impact of carrier status determination for Duchenne/Becker muscular dystrophy by computer-assisted laser densitometry
3. The frequency of patients with dystrophin abnormalities in a limb-girdle patient population
4. Accurate and rapid detection of heterozygous carriers of a deletion by combined polymerase chain reaction and high-performance liquid chromatography.
5. Germline mosaicism and Duchenne muscular dystrophy mutations
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1. Evaluation of Left-Sided Heart Chambers With Novel Echocardiographic Techniques in Men With Duchenne or Becker Muscular Dystrophy;The American Journal of Cardiology;2019-03
2. Cost-Effectiveness Analysis of Diagnosis of Duchenne/Becker Muscular Dystrophy in Colombia;Value in Health Regional Issues;2018-12
3. Predictors of early left ventricular systolic dysfunction in duchenne muscular dystrophy patients;Muscle & Nerve;2018-03-01
4. MLPA identification of dystrophin mutations and in silico evaluation of the predicted protein in dystrophinopathy cases from India;BMC Medical Genetics;2017-06-13
5. Expression levels of TGF-β1 and CTGF are associated with the severity of Duchenne muscular dystrophy;Experimental and Therapeutic Medicine;2017-02-07
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