Did you miss the recent Devyser webinar with Dr. Robert Akkers highlighting the shifting distribution of hemoglobinopathy and the need for expanded thalassemia genetic testing? Now watch the on-demand webinar here: https://bit.ly/3RPitjr #thalassemia #ngs #genetictesting
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Register for our upcoming webinar with Dr. Robert Akkers highlighting the shifting distribution of hemoglobinopathy, and the need for expanded thalassemia genetic testing. Register today —>https://bit.ly/4eq6OBr #Thalassemia #Genetic #hemoglobinopathy
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New Episode of ASN Kidney Translation with @Nephro_Sparks @ASNKidney Genetic Testing in Nephrology: Topics include genetic testing in CKD, MUC1 ADTKD screening, and digenic Alport syndrome insights https://lnkd.in/e2gFnjAq
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Our paper on genetic testing of VEXAS syndrome has recently been published. You can read the paper and let us know if you have the testing needs. #vexas #xna #luminex https://lnkd.in/g4egwu9h
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Pharmacogenomics expert, psychiatric pharmacist, and strategic thinker with a passion for education, developing strong relationships, and leadership.
DPYD PGx testing is an easy way to ensure you get the right dose of fluorouracil-based chemotherapy. It may not be part of clinical guidelines, but when DPYD testing has such a high level of evidence, it should be.
DPYD genetic variants could cause severe adverse effects and even death. DPYD Pharmacogenomic testing is currently in the guidelines for 5 Fluorouracil , Capecitabine and Tegafur. Ask your oncologist for genetic testing options. https://lnkd.in/grB4zFda
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DPYD genetic testing is crucial before the administration of 5-FU, capecitabine and tegafur.🙌🤞Stay on a safe side✅
DPYD genetic variants could cause severe adverse effects and even death. DPYD Pharmacogenomic testing is currently in the guidelines for 5 Fluorouracil , Capecitabine and Tegafur. Ask your oncologist for genetic testing options. https://lnkd.in/grB4zFda
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Hereditary Genetic Testing Market to Soar to $81.95 Billion by 2033: BIS Research https://lnkd.in/eWV5D86Z #marketanalysis #marketresearch #marketresearchreports #businessintelligence
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Through the Open Hyperinsulinism Genes Project - a collaboration with The University of Exeter, we have been able to provide testing to 894 individuals from 61 different countries! This program offers free genetic testing services to those diagnosed with hyperinsulinism. To learn more about our partnership, visit https://bit.ly/chi-exeter #hyperinsulinism #raredisease #congenitalhyperinsulinism #hypoglycemia | Hyperinsulinism | Congenital | HI | Hypoglycemia | Rare Disease
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Introducing MedGenome’s BabySecure Lysosomal Storage Disorders (LSD) Panel! This test detects a diverse group of Lysosomal Storage Disorders (LSDs) through enzyme activity assays using Liquid Chromatography–Mass Spectrometry (LC-MS). By identifying genetic mutations early, we help ensure your baby receives the right support and care from the very beginning. Give your little one the best start with BabySecure! For more information, reach us at 1800 296 9696 or email diagnostics@medgenome.com #MedGenome #Genetics #BabySecure #NewbornScreeningTest
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Do you want to use ClinVar to better understand genetic testing results? Check out GenomeConnect’s recent webinar “ClinVar - How to Search and How to Track a Variant” ⬇️ https://ow.ly/2XTW50U2BmK
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