Last Posted: Sep 10, 2020
- Categorized Genetic Analysis in Childhood-Onset Cardiomyopathy.
Al-Hassnan Zuhair N et al. Circulation. Genomic and precision medicine 2020 Sep - Clinical Utility of a Phenotype Enhanced MYH7 -Specific Variant Classification Framework in Hypertrophic Cardiomyopathy Genetic Testing.
Mattivi Connor L et al. Circulation. Genomic and precision medicine 2020 Sep - Precision Medicine for Breast Cancer Utilizing Circulating Tumor DNA: It Is in the Blood.
Miller Emily et al. Current treatment options in oncology 2020 Sep 21(11) 89 - Predicting progression to advanced age-related macular degeneration from clinical, genetic and lifestyle factors using machine learning.
Ajana Soufiane et al. Ophthalmology 2020 Sep - Founder Mutation in N-terminus of Cardiac Troponin I Causes Malignant Hypertrophic Cardiomyopathy.
Fahed Akl C et al. Circulation. Genomic and precision medicine 2020 Sep - [Clinical phenotype of Alport syndrome in monozygotic twins].
Deng H Y et al. Zhonghua er ke za zhi = Chinese journal of pediatrics 2020 Sep 58(9) 731-737 - Genomic Testing for Relapsed and Refractory Lymphoid Cancers: Understanding Patient Values.
Costa Sarah et al. The patient 2020 Sep - How to use precision medicine to personalize COVID-19 treatment according to the patient’s genes
C Allen et al, The Conversation, September 1, 2020 - Improving Community Advisory Board Engagement in Precision Medicine Research to Reduce Health Disparities.
Connors Erin et al. Journal of health disparities research and practice 2019 12(6) 80-94 - Moving Genomics to Routine Care: An Initial Pilot in Acute Cardiovascular Disease.
Aryan Zahra et al. Circulation. Genomic and precision medicine 2020 Aug
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