Unlocking the genetic blueprint of duchenne muscular dystrophy: A personalized approach with MLPA and WES.
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- Global Medical Genetics, 2025, v. 12, n. 2, p. 1, doi. 10.1016/j.gmg.2025.100038
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- Article
Works matching AU Agarwal, Kamlesh
Results: 7
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Limb-Girdle Muscular Dystrophies (LGMD): Clinical features, diagnosis and genetic variability through next generation sequencing.
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- Global Medical Genetics, 2025, v. 12, n. 1, p. 1, doi. 10.1016/j.gmg.2024.100035
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- Article
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Synthesis and reactions of heterocyclic 2,3-epoxypropionitriles with pyrrolidine.
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- Journal of Heterocyclic Chemistry, 1987, v. 24, n. 1, p. 15, doi. 10.1002/jhet.5570240103
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- Article
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Synthesis and reactions of heterocyclic methyl 2-propenoates and 2,3-epoxypropanoates with nucleophiles.
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- Journal of Heterocyclic Chemistry, 1985, v. 22, n. 1, p. 65, doi. 10.1002/jhet.5570220117
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- Article
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Screening for Gaucher's disease in unexplained spleenomegaly and/or thrombocytopenia: An observational study.
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- Journal of Medical & Allied Sciences, 2021, v. 11, n. 2, p. 120, doi. 10.5455/jmas.2070
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- Article
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Duchenne Muscular Dystrophy: Genetic and Clinical Profile in the Population of Rajasthan, India.
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- Annals of Indian Academy of Neurology, 2021, v. 24, n. 6, p. 873, doi. 10.4103/aian.AIAN_126_21
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- Article
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A Study of Sick Newborn for Inborn Error of Metabolism by Tandem Mass Spectrometry.
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- Journal of Neonatology, 2022, v. 36, n. 2, p. 125, doi. 10.1177/09732179221100447
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- Article