Pasch, Andreas (2010). [Early genetic testing in nephrology - a diagnostic aid in ambiguous clinical situations]. Therapeutische Umschau, 67(7), pp. 375-80. Bern: Huber
Full text not available from this repository. (Request a copy)Despite a growing number of identified genetic causes of monogenetic disorders, early molecular testing is rarely applied in daily nephrologic practice. In selected cases and to answer specific questions, molecular testing however can be helpful for the specialist. The future significance of genetic testing most likely lies in the area of individual risk profiling for polygenetic disorders. The basis for this testing however has yet to be established.
Item Type: |
Journal Article (Further Contribution) |
|---|---|
Division/Institute: |
04 Faculty of Medicine > Department of Dermatology, Urology, Rheumatology, Nephrology, Osteoporosis (DURN) > Clinic of Nephrology and Hypertension |
UniBE Contributor: |
Pasch, Andreas |
ISSN: |
0040-5930 |
Publisher: |
Huber |
Language: |
German |
Submitter: |
Factscience Import |
Date Deposited: |
04 Oct 2013 14:11 |
Last Modified: |
05 Dec 2022 14:01 |
PubMed ID: |
20577966 |
URI: |
https://boris.unibe.ch/id/eprint/1789 (FactScience: 203815) |
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