Found: 5
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The diagnosis of inherited metabolic diseases by microarray gene expression profiling.
- Published in:
- Orphanet Journal of Rare Diseases, 2010, v. 5, p. 34, doi. 10.1186/1750-1172-5-34
- By:
- Publication type:
- Article
Impact of pharmacogenomic DPYD variant guided dosing on toxicity in patients receiving fluoropyrimidines for gastrointestinal cancers in a high-volume tertiary centre.
- Published in:
- BMC Cancer, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12885-023-10857-8
- By:
- Publication type:
- Article
Adenine phosphoribosyltransferase deficiency in the United Kingdom: two novel mutations and a cross-sectional survey.
- Published in:
- Clinical Kidney Journal, 2016, v. 9, n. 6, p. 800, doi. 10.1093/ckj/sfw093
- By:
- Publication type:
- Article
The contribution of deleterious DPYD gene sequence variants to fluoropyrimidine toxicity in British cancer patients.
- Published in:
- Cancer Chemotherapy & Pharmacology, 2010, v. 65, n. 2, p. 403, doi. 10.1007/s00280-009-1147-x
- By:
- Publication type:
- Article
Autosomal dominant tubulointerstitial kidney disease-UMOD is the most frequent non polycystic genetic kidney disease.
- Published in:
- 2018
- By:
- Publication type:
- journal article