Precision Medicine for Continuing Phenotype Expansion of Human Genetic Diseases
Joint Authors
Source
Issue
Vol. 2015, Issue 2015 (31 Dec. 2015), pp.1-4, 4 p.
Publisher
Hindawi Publishing Corporation
Publication Date
2015-06-07
Country of Publication
Egypt
No. of Pages
4
Main Subjects
Abstract EN
Determining the exact genetic causes for a patient and providing definite molecular diagnoses are core elements of precision medicine.
Individualized patient care is often limited by our current knowledge of disease etiologies and commonly used phenotypic-based diagnostic approach.
The broad and incompletely understood phenotypic spectrum of a disease and various underlying genetic heterogeneity also present extra challenges to our clinical practice.
With the rapid adaptation of new sequence technology in clinical setting for diagnostic purpose, phenotypic expansions of disease spectrum are becoming increasingly common.
Understanding the underlying molecular mechanisms will help us to integrate genomic information into the workup of individualized patient care and make better clinical decisions.
American Psychological Association (APA)
Yu, Hui& Zhang, Victor Wei. 2015. Precision Medicine for Continuing Phenotype Expansion of Human Genetic Diseases. BioMed Research International،Vol. 2015, no. 2015, pp.1-4.
https://search.emarefa.net/detail/BIM-1056590
Modern Language Association (MLA)
Yu, Hui& Zhang, Victor Wei. Precision Medicine for Continuing Phenotype Expansion of Human Genetic Diseases. BioMed Research International No. 2015 (2015), pp.1-4.
https://search.emarefa.net/detail/BIM-1056590
American Medical Association (AMA)
Yu, Hui& Zhang, Victor Wei. Precision Medicine for Continuing Phenotype Expansion of Human Genetic Diseases. BioMed Research International. 2015. Vol. 2015, no. 2015, pp.1-4.
https://search.emarefa.net/detail/BIM-1056590
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-1056590