Last Posted: Oct 24, 2019
- One Little Girl’s Story Highlights the Promise of Precision Medicine
F Collins, NIH director's blog, October 23, 2019 - The use or generation of biomedical data and existing medicines to discover and establish new treatments for patients with rare diseases - recommendations of the IRDiRC Data Mining and Repurposing Task Force.
Southall Noel T et al. Orphanet journal of rare diseases 2019 Oct 14(1) 225 - Toward Clinical Implementation of Next-Generation Sequencing-Based Genetic Testing in Rare Diseases: Where Are We?
Liu Zhichao et al. Trends in genetics : TIG 2019 Oct - Current status of biomarker testing in historically rare, high-unmet-need tumors: soft tissue sarcomas and thyroid cancers.
Schroader Bridgette et al. Expert review of anticancer therapy 2019 Oct - NIH's All of Us Partners with HudsonAlpha on Long-Read Sequencing Project
Clinical Omics, October 18, 2019 - Every Diagnosis Matters
Global Genes, October 17, 2019 - She began to talk ? then mysteriously fell silent. Months later her parents learned why
SG Boodman, The Washington Post, October 12, 2019 - Genomic testing in healthcare: a hybrid space where clinical practice and research need to co-exist.
Horton Rachel et al. Expert review of molecular diagnostics 2019 Oct 1-5 - Heritable Genome Editing: Who Speaks for "Future" Children?
Knoppers Bartha Maria et al. The CRISPR journal 2019 Oct 2(5) 285-292 - A Drug Was Made For Just One Child, Raising Hopes About Future Of Tailored Medicine
A Chen, WBUR, October 11, 2019
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