Application of a reliable and rapid polymerase chain reaction based method in the diagnosis of myotonic dystrophy type 1 (DM1) in India
Author:
Funder
DBT, New Delhi
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
Reference22 articles.
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3. An unstable triplet repeat in a gene related to myotonic muscular dystrophy;Fu;Science,1992
4. Diagnostic efficiency, embryonic development and clinical outcome after the biopsy of one or two blastomeres for preimplantation genetic diagnosis;Goossens;Hum. Reprod.,2008
5. A rapid polymerase chain reaction-based test for screening Steinert's disease (DM1);Hamzi;Neurol. India,2010
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2. CpG methylation and various parameters interaction in myotonic dystrophy type 1;Journal of Analytical & Pharmaceutical Research;2020
3. Myotonic Dystrophies;Neuromuscular Disorders;2017-12-28
4. Haplotype analysis and LD detection at DM1 locus;Gene;2015-08
5. Molecular genetic analysis of trinucleotide repeat disorders (TRDs) in Indian population and application of repeat primed PCR;European Journal of Medical Genetics;2015-03
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