Probably Genetic

Rare genetic conditions can take years for doctors to diagnose. #ProbablyGenetic is a personalized healthcare company working to help you find answers.

[Probably Genetic @ProbGenetic]

We are offering no-cost genetic testing for individuals with pediatric-onset seizure and movement disorders. If you or a loved one experience seizures, movement difficulties, or have received a cerebral palsy diagnosis apply for testing here: https://t.co/DTu7tFL7Xa

[Effie Parks @OnceUponAGene]

We are so excited to partner with @ProbGenetic
Their FREE #genetictesting program includes genetic counseling.
https://t.co/MDtFsBgoF4
If you know someone with #cerebralpalsy or #epilepsy who has not had whole exome sequencing, PLEASE share this with them!
#CTNNB1

[Probably Genetic @ProbGenetic]

Congrats to @JMGraglia and the @cureSYNGAP1 team for getting covered in Newsweek!

If you want to understand what it means to be undiagnosed, to get a diagnosis for a condition without a treatment, and to make people take on your cause and work on therapeutics, read this article.

[CURE SYNGAP1 aka SynGAP Research Fund 501(C)(3) @cureSYNGAP1]

Read & share this @Newsweek story profiling SRF, our founders (@SYNGAP1mom & @JMGraglia) and Tony's diagnostic journey.

https://t.co/eyWvSifnaL

FYI @StanfordChild @IDreamofGenes @Invitae @Labcorp (MNG)

[Bluefield Project @BluefieldProj]

We have partnered with @ProbGenetic to launch a US-based, no-cost genetic testing program for eligible individuals diagnosed with #FTD or experiencing FTD-like symptoms. If you or anyone in your community might benefit from this opportunity, please see https://t.co/dqFiirtvGh

[Probably Genetic @ProbGenetic]

Meet our Associate Product Manager! #ProbablyGenetic

[Probably Genetic @ProbGenetic]

Meet Jancie!

[Probably Genetic @ProbGenetic]

Probably Genetic has had quite a few new hires recently! We are thrilled to be adding to our team. ⁣Stay tuned for future posts to get to know our team of dedicated individuals!

[Probably Genetic @ProbGenetic]

Most, but not all, genetic disorders begin in childhood. The frequency of childhood genetic disorders is under recognized, yet awareness is imperative for early intervention and treatment. That’s why Probably Genetic makes it our goal to shorten the diagnostic odyssey! #Genetics

[Probably Genetic @ProbGenetic]

Follow us on Instagram! #ProbablyGenetic #Instagram

[CURE SYNGAP1 aka SynGAP Research Fund 501(C)(3) @cureSYNGAP1]

PRESS RELEASE:
SynGAP Research Fund deploys #CouldItBeSYNGAP1 screening tool in partnership with @ProbGenetic! Share this tool with #epilepsy #autism and other #specialneeds communities.
#SYNGAP1
https://t.co/wxvfHYirWj

[Probably Genetic @ProbGenetic]

Did you know? • #RareDisease affects 350 million people worldwide. 🌎

[Probably Genetic @ProbGenetic]

Understanding the lives of #raredisease patients is imperative for those researching and developing treatments for rare diagnoses. ➤ https://t.co/3pydQxTGRV

[Probably Genetic @ProbGenetic]

Why Drug Developers Are Launching Sponsored Testing Programs With Probably Genetic https://t.co/KhuLkQL2JB

[Probably Genetic @ProbGenetic]

It’s Global Niemann-Pick Awareness Day.

[Probably Genetic @ProbGenetic]

Meet @hospitalprncss, our Patient Community Manager!

[Probably Genetic @ProbGenetic]

Meet our CTO!

[Probably Genetic @ProbGenetic]

Did you know 50% of all rare disease patients are children? #FactFriday

[Probably Genetic @ProbGenetic]

Meet our BD Associate!

[Probably Genetic @ProbGenetic]

Meet our software developer! 💻

[Probably Genetic @ProbGenetic]

Meet our CEO!