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CeGaT Exome Xtra - available as of today! This latest diagnostic
#innovation developed by CeGaT is the most powerful#genetic diagnostic tool for patients with complex and unspecific diseases, helping physicians make a#diagnosis.#launch https://bit.ly/380ki4q pic.twitter.com/0Fq6XPiPPb
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Today is World Cancer Day. We would like to help raise awareness of the importance of cancer research - it brings forward the day when hopefully all cancers can be cured.
#WorldCancerDay2020
#CancerAwarenesspic.twitter.com/Q2grZA8s4v
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Read CeGaT's recent paper on single gene testing: "Novel MECP2 Mutation c.1162_1172del p.Pro388 in Two Patients with Symptoms of Atypical Rett Syndrome." https://bit.ly/37Tqhbb
#genetictesting#geneticspic.twitter.com/QHJ21xzjTl
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CeGaT offers premium
#genetic#diagnostics - worldwide. As we are committed to long-term, reliable collaborations, regular exchange of information is very important to us. Therefore, we currently meet with our partner Fugene and many medical doctors in Israel - many#greetings!pic.twitter.com/IBMK7JJqgW
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A few team figures: In the last decade, our team has grown a hundredfold. The age range goes from 23 to 61 years; 69 percent of us are women. Almost one in two has a Ph.D.
#10years10facts#genetics#team https://www.cegat.de/en/about-cegat/team/ …pic.twitter.com/I09RvJk8pD
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The CeGaT building is only 100 meters away from where CeGaT rented its first labs. Our own building was completed in 2014. And because CeGaT is growing so fast, an extension of the building is planned in the near future.
#10years10facts#genetics https://bit.ly/2R8HFTa pic.twitter.com/rzep11CZAg
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Read CeGaT's recent paper on genetic eye diseases: "Ophthalmic features of retinitis pigmentosa in Cohen syndrome caused by pathogenic variants in the VPS13B gene." https://bit.ly/2R4sL0q
#genetictesting#eyediseases#geneticspic.twitter.com/tSNa3uFRri
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Our first genetic diagnostic panels were the Panel for Epilepsy and the Panel for
#Genetic Eye Diseases, covering in total 155 genes in 2010. After many updates, according to#scientific progress, they include more than 1000 genes in 2020#10years10facts https://bit.ly/36SsoLT pic.twitter.com/buNFtBSWC8
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CeGaT GmbH proslijedio/la je Tweet
Despite having no cure, an early diagnostic test could significantly improve the quality of life for the 10 million people living with Parkinson’s Disease. Neuroscientists think they might be on the right track: https://buff.ly/3946whY pic.twitter.com/tYisMdWI2L
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CeGaT GmbH proslijedio/la je Tweet
Learning More About the Migration of Metastatic Cancer Cells | Cancer cells want to conserve energy as they migrate to different parts of the body, new work has shown. https://buff.ly/34n8kPx pic.twitter.com/Dah0cdRmOc
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When CeGaT was founded in 2009, we started as a
#diagnostic service provider. Today, we support not only physicians and their patients, but also science and the#pharmaceutical industry with a broad service portfolio.#10years10facts#genetics https://bit.ly/2NpqE59 pic.twitter.com/gsYQLuWa5j
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A somewhat unusual set of figures for the
#annualreport: Last year, we consumed over 400 kg of#coffee and over 1.5 tons of#fruit in the office. That is over 2 kg of coffee and over 7.5 kg of fruit per person.#10years10facts https://www.cegat.de/en/ pic.twitter.com/6uBnj8DCtu
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2019 was special for us: It marked the 10th anniversary of CeGaT. We are grateful for the experiences we made and proud of what we have achieved. Reason enough to look back and share a few facts with you that you probably did not know yet.
#10years#10facts#anniversary#lookbackpic.twitter.com/FQKDNuo62Z
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Read CeGaT's recent paper on
#brain development#disorders: "Novel synonymous and missense variants in FGFR1 causing Hartsfield syndrome."#genetics https://bit.ly/2EcUMM2 pic.twitter.com/oIBOtYQktf
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CeGaT has updated the Panel for
#KidneyDisease according to scientific findings and increased its#diagnostic sensitivity. 30 new#genes that have been identified in studies as possible causes of#renaldiseases are now included in the panel's gene sets. https://bit.ly/360PfUC pic.twitter.com/8rSKeVrXKD
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Greetings from
#Switzerland! We are currently at the#GenomicsLIVE 2019 in Basel. Meet us and learn more about CeGaT’s product portfolio.#genetics#genetictestingpic.twitter.com/VFbZyjtkl5
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CeGaT has expanded its business unit for the realization of
#scientific projects: “Research and Pharmas Solutions” offers a broad portfolio of#sequencing services and tumor analyses to generate the data basis for clinical studies and#medical innovations. https://www.cegat.de/en/services/ pic.twitter.com/RWyDufba3v
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CeGaT GmbH proslijedio/la je Tweet
Genetic conditions may increase the risk of stomach cancer, such as a mother, father, sister, or brother who has had stomach cancer, having Type A blood, Li-Fraumeni syndrome, Familial adenomatous polyposis (FAP) or Lynch syndrome. http://bit.ly/2Ouhvbc pic.twitter.com/L7YWyBVLMF
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CeGaT is at the 16º Congresso Nacional de Oncologia. It is taking place in
#Estoril, Portugal, from November 28–30, 2019. Come and talk to Sami Azrak, PhD about CeGaT's#tumor#diagnostics.#genetictesting https://bit.ly/2L2LQfV pic.twitter.com/D0zfBS5vSu
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