Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Precision Health Database


Genomics & Health Impact Scan Database|Search|PHGKB

Rare Diseases

Last data update: Mar 23, 2023. (Total: 58888 Documents since 2012)
   dataset      
Filtered By:

Previous    

Records 1 - 7 (of 7 Records)

Query Trace: Duchenne Muscular Dystrophy[original query]>>Tools/Methods [Product Type]
Duchenne Muscular Dystrophy Education Series
American Academy of Pediatrics
New CRISPR tool has the potential to correct almost all disease-causing DNA glitches, scientists report
S Begley. Stat News, October 21, 2019
A checklist for clinical trials in rare disease: obstacles and anticipatory actions-lessons learned from the FOR-DMD trial.
Crow Rebecca A et al. Trials 2018 May 19(1) 291
DMD Open-access Variant Explorer (DOVE): A scalable, open-access, web-based tool to aid in clinical interpretation of genetic variants in the DMD gene.
Bailey Mitchell et al. Molecular genetics & genomic medicine 2018 Nov
DMDtoolkit: a tool for visualizing the mutated dystrophin protein and predicting the clinical severity in DMD.
Zhou Jiapeng et al. BMC bioinformatics 2017 Feb 18(1) 87
Clinical Follow-Up For Duchenne Muscular Dystrophy Newborn Screening: A Proposal.
Kwon Jennifer M et al. Muscle & nerve 2016 May
The TREAT-NMD Duchenne muscular dystrophy registries: conception, design, and utilization by industry and academia.
TOP