¡Marque sus calendarios para nuestro próximo CentoTalk! 📅
Regístrese ahora para saber cómo los biomarcadores multiómicos pueden ayudarlo a diagnosticar a su paciente con la enfermedad de Niemann-Pick: t.co/q9yXMGBAjk t.co/Ysjz86n3Da
Casi el 4% de los recién nacidos nacerán con una enfermedad genética o un defecto congénito importante.
Vea nuestro último CentoTalk para conocer las opciones de pruebas #prenatales más tempranas y precisas disponibles para usted y sus #pacientes:
Mark your calendars for our upcoming #CentoTalk! 📅
Register now for this interactive #webinar to learn how #multiomic #biomarkers can help you diagnose your #NiemannPick disease #patient:
Nearly 4% of newborns will be born with a #genetic disease or major birth defect.
Watch our latest on-demand CentoTalk today to learn about the earliest and most accurate #PrenatalTesting options available for you and your patients: t.co/ybHTzriO4X
#Webinar #CentoTalk t.co/pFWd8jfe9Z
𝙉𝙀𝙒𝙎: CENTOGENE Discovers Six New Rare Diseases by Leveraging the Strength of Its Bio/Databank.
Read more in @TheACMG’s Genetics in Medicine to see how we diagnosed over 90 patients & opened up treatment options: t.co/V3r03jgFvo
#Genetics #Research #RareDisease t.co/WlxPTVOcos
It’s almost here!
24 hours to go until the May edition of our monthly #newsletter & a look at six new #RareDiseases recently discovered at CENTOGENE
Subscribe now to learn about our #news in rare disease #diagnostics, #research, & #OrphanDrug development: t.co/wVPJPbCSxx t.co/4bguImBjIM
@BWHNeurology @ParkinsonDotOrg #Fabry disease affects millions of people around the world. Together, we are rare! #FabryAwarenessMonth