Personalized Management of Genetic Disorders
Author:
Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-030-62080-6_16
Reference35 articles.
1. Aguiar P, Azevedo O, Pinto R, et al. New biomarkers defining a novel early stage of Fabry nephropathy: a diagnostic test study. Mol Genet Metab. 2017;121:162–9.
2. Amaral MD. Novel personalized therapy for cystic fibrosis: treating the basic defect in all patients. J Intern Med. 2015;277:155–66.
3. Auray-Blais C, Lavoie P, Tomatsu S, et al. UPLC-MS/MS detection of disaccharides derived from glycosaminoglycans as biomarkers of mucopolysaccharidoses. Anal Chim Acta. 2016;936:139–48.
4. Bianchi DW, Parker RL, Wentworth J, et al. DNA sequencing versus standard prenatal aneuploidy screening. N Engl J Med. 2014;370:799–808.
5. De Lellis L, Curia MC, Veschi S, et al. Methods for routine diagnosis of genomic rearrangements: multiplex PCR-based methods and future perspectives. Expert Rev Mol Diagn. 2008;8:41–52.
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