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First Genomix

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Al Razi Building 64 Block E, 1st Floor, Offices 129-130-131 - Dubai Healthcare City
333410 Dubai, United Arab Emirates
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First Genomix Company Bio

General information

The industry in which First Genomix operates is medical laboratory. The country where First Genomix is located is United Arab Emirates, while the company's headquarters is in Dubai.

Unfortunately, we do not have detailed information about the company's offer and products, therefore we suggest you to send a request for information or contact by phone: +97143443222

You can visit the headquarters of First Genomix. If you want to reach it, go to the address: Al Razi Building 64 Block E, 1st Floor, Offices 129-130-131 - Dubai Healthcare City, 333410 Dubai, United Arab Emirates.

Use the geographic coordinates of the company location: 25.04786, 55.15076, to easily reach the given address using GPS navigation.

Al Razi Building 64 Block E, 1st Floor, Offices 129-130-131 - Dubai Healthcare City Dubai

Opening hours
Monday:
9:00 - 21:00
Tuesday:
9:00 - 21:00
Wednesday:
9:00 - 21:00
Thursday:
9:00 - 21:00
Friday:
9:00 - 21:00
Saturday:
9:00 - 21:00
Sunday:
9:00 - 21:00
Phone numbers
+97143443222 (Main)
Websites
https://firstgenomix.ae
Establishment year
2012
Activity form
Services
Categories
medical laboratory
Keywords
genetic testing dubai, genetic screening, genetic solutions

Videos

  • Non-invasive prenatal testing (NIPT) is a safe and highly advanced screening tool that provides an early insight into your baby's genetic health. From 10 weeks only, NIPT can analyze cell-free DNA from maternal blood to screen the baby for common chromosomal disorders such as Down syndrome. Performing NIPT early gives you the peace of mind you need and enables you to consider your options carefully in the future. The NIPT test by First Genomix is complemented by genetic counseling support that helps carefully walk expecting couples through the whole testing process, providing guidance and support every step of the way. First Genomix is a renowned name that has pioneered the use of Next-Generation Sequencing technology in the GCC and Middle East, providing cutting-edge diagnostic services in reproductive, prenatal, and diagnostic genetics since 2012. Ensure the well-being of your baby today with NIPT (Non-Invasive Prenatal Testing) by First Genomix and continue your journey to parenthood with more peace and joy. Visit https://nipt.ae to schedule your NIPT appointment today. #FirstGenomix #NIPT #PrenatalTesting #HealthyPregnancy #downsyndrome #geneticcounseling #trisomy21
  • A deep dive into the realm of genetic health and testing. In this inaugural episode, hosted by Dany Mohsen, we explore the world of Non-Invasive Prenatal Testing (NIPT) - a revolutionary approach in prenatal screening. As the name suggests, NIPT is a non-invasive method that provides crucial information about a baby's genetic health long before its arrival, a subject of utmost importance to expectant parents and medical professionals alike. The host, Dany Mohsen, engages in a thought-provoking discussion with Clinical Scientist ‘Matthew Wyatt’ who delves into the reasons of why NIPT testing is important, the procedural aspects, and why First Genomix is the preferred choice for this service. Expectant parents or couples planning to start a family can benefit significantly from this discussion, helping them gain insights into how NIPT results can guide critical decisions in the future. Likewise, healthcare professionals can gain a deeper understanding about the clinical utility of NIPT in modern obstetrics. This podcast serves as an informative guide, breaking down complex genetic information into digestible and easy-to-understand insights. Tune in for a comprehensive and exciting discussion about NIPT on our first-ever episode of “Genetic Mysteries Unravelled” by First Genomix.
  • Are you planning a family? Your first step starts here. This video introduces you to the concept of Carrier Screening – a crucial, yet simple, genetic test that could ensure the health of your future children. With FirstScreen by First Genomix, a comprehensive Carrier Screening panel test, we offer an in-depth look at the potential recessive genetic disorders you and your partner may be silent carriers of. This advanced DNA Sequencing Technology delves into approximately 2950 genes from just a small sample of blood to check for any disease-causing mutations. But we don't just leave you with a bunch of scientific terms. At First Genomix, you have access to genetic counselling support, both before and after the test, guiding you through your results and understanding your future reproductive options. Our video is a crucial step in making the right decisions for your family's future health. Get excited about finding solutions and creating a healthy family. Be informed, be prepared, and secure a healthier future for your children.
  • Welcome back to the second episode of “Genetic Mysteries Unravelled” by First Genomix, where we continue our exploration of the world of genetic health and testing. In this enlightening episode, we unravel the fascinating science behind FirstScreen (Carrier Screening) – a crucial genetic test that holds the power to shape the future of our families and our health. FirstScreen (Carrier Screening) allows individuals to understand their genetic makeup better and be aware of potential genetic conditions that they might pass on to their children. Our host, Dany Mohsen, in conversation with Zeina Younes, the Deputy Head of Genetic Diagnostics Department, discusses what it means to be a silent carrier of genetic conditions, why it's important for every individual, particularly couples planning to start a family, to undergo carrier screening, and how this can help identify the risks of having affected offspring. Discover intriguing insights about the increased risk among related couples, the recurring percentage of risk in each pregnancy, and the kind of diseases that this test can potentially reveal. Zeina also explains the process of the test, the potential solutions for couples sharing a mutation in the same gene, and why First Genomix stands as the preferred choice for carrier screening. This episode is a must-watch for anyone who wants to understand the impact of our genes on our health, or those looking to make informed decisions about starting a family. Don't miss this chance to gain a deeper understanding of carrier screening and the powerful role it plays in our lives. #FirstScreen #CarrierScreening #Podcast #FirstGenomix #GeneticMysteries
  • October is synonymous with Breast Cancer Awareness, and in honor of the brave women fighting this battle and the previvors who understand their hereditary risk, Dany Mohsen brings you an insightful podcast on this critical topic featuring Dr. Sama Zibdeh, a renowned breast oncoplastic surgeon at Emirates Hospital, and Sahar Abdelaziz, Geneticist at First Genomix, to share their expertise on this crucial topic. In the podcast, Dany guides an in-depth exploration into the realm of breast cancer through his special guests, offering a comprehensive look at genetic testing for breast cancer, its indications, and implications. In the episode, the speakers also delve into the clinical symptoms of the disease, the essential screening procedures, and the prophylactic surgeries for high-risk individuals. Moreover, the pivotal role of genetic counseling in providing both psychological support and clarity is also emphasized. But the podcast doesn’t end there. The experts also provide a thorough investigation into the genetic connections between breast cancer and other hereditary cancers, underlining the importance of genetic testing for families with a history of such diseases. Tune in with Dany and his guests in this special episode and be part of the awareness change today!

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