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1.
Confirmation of Insertion, Deletion, and Deletion-Insertion Variants Detected by Next-Generation Sequencing.
Clin Chem
; 69(10): 1155-1162, 2023 10 03.
Article
in English
| MEDLINE | ID: mdl-37566393
2.
Point of care CYP2C19 genotyping after percutaneous coronary intervention.
Pharmacogenomics J
; 22(5-6): 303-307, 2022 12.
Article
in English
| MEDLINE | ID: mdl-35449399
3.
Genetic and biochemical analyses in dyslipidemic patients undergoing LDL apheresis.
J Clin Apher
; 29(5): 256-65, 2014 Oct.
Article
in English
| MEDLINE | ID: mdl-24420163
4.
Genetic variation in statin intolerance and a possible protective role for UGT1A1.
Pharmacogenomics
; 19(2): 83-94, 2018 Jan.
Article
in English
| MEDLINE | ID: mdl-29210320
5.
Technical Advances for the Clinical Genomic Evaluation of Sudden Cardiac Death: Verification of Next-Generation Sequencing Panels for Hereditary Cardiovascular Conditions Using Formalin-Fixed Paraffin-Embedded Tissues and Dried Blood Spots.
Circ Cardiovasc Genet
; 10(6)2017 Dec.
Article
in English
| MEDLINE | ID: mdl-29237689
6.
Preemptive Pharmacogenomic Testing for Precision Medicine: A Comprehensive Analysis of Five Actionable Pharmacogenomic Genes Using Next-Generation DNA Sequencing and a Customized CYP2D6 Genotyping Cascade.
J Mol Diagn
; 18(3): 438-445, 2016 05.
Article
in English
| MEDLINE | ID: mdl-26947514
7.
LDLR promoter variant and exon 14 mutation on the same chromosome are associated with an unusually severe FH phenotype and treatment resistance.
Eur J Hum Genet
; 17(1): 85-90, 2009 Jan.
Article
in English
| MEDLINE | ID: mdl-18648394
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