RareDiseaseGenomicsRSA
@raregenomicsrsa
"Until every African patient with a Rare Disease is diagnosed!" Research group at Stellenbosch University, directed by Prof Shahida Moosa @shahida_moosa
ID: 1315689708953972736
12-10-2020 16:24:28
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830 Followers
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Congratulations Prof Shahida Moosa #StopTheGenocide 🥳🥳🥳
1st seminar #GenomicsForHealthInAfrica #AfricaEuropeCoRE Prof Shahida Moosa #StopTheGenocide on: "Impact of Clinical Genomics in Africa" - where we started&where we're going -> from Southern Africa > Central Africa & beyond! We are #hiring! PostDocs apply now! SU, Faculty of Medicine and Health Sciences ARUA The Guild
📢We're hiring! Another #PostDoc position is available in our group. Interested in #RareDiseases or #Cancer? The successful #PostDoc will be instrumental in our #AfricaEuropeCoRE called #GenomicsForHealthInAfrica SU, Faculty of Medicine and Health Sciences Division of Molecular Biology and Human Genetics Stellenbosch University Postdocs Tygerberg Postgraduate Student Council (TPSC) Research at Stellenbosch University
Pls RT We have a #postdoc fellowship within the #GenomicsForHealthInAfrica #AfricaEuropeCoRE Come and make an impact on the millions of Africans living with #RareDiseases and #Cancer The RareDiseaseGenomicsRSA team is amazing, as are all our collaborators in the MAGIC lab in the #BMRI
CELEBRATING SCIENTIFIC EXCELLENCE! CONGRATULATIONS to Profs Shahida Moosa #StopTheGenocide, Nelita du Plessis, Mark Tomlinson, Bob Nash, and Dr Yoshan Moodley, who were all awarded at the SA SAMRC's 10th #ScientificMeritAwards. We couldn’t be more proud! READ MORE here: bit.ly/49To0Nc.
Happy birthday to little C - she is so sweet and so clever! 🥳😍🥰 Everything of the best for you and your wonderful mom Thandokazi Mvelashe
🤩 Lightning-speed diagnosis of a complex undiagnosed family! -->1 more diagnosed family (with 2 different disorders!) Thank you *Carli*, for fulfilling: "Until every African with a #RareDisease is diagnosed!" Carli started MSc in February, can you believe it? Shahida Moosa #StopTheGenocide
RT Francisco Martínez: Pathogenic variants in HGF give rise to childhood-to-late onset primary lymphoedema by loss of function. #RareDisease #Genetics #morbidgene academic.oup.com/hmg/advance-ar…
Michael (name giver of Michael Foundation and #epilepsy Michael Prize) probably had #williamssyndrome. link.springer.com/article/10.100… This post-mortem diagnosis is based on dysmorphologic and clinical analysis & AI (GestaltMatcher (.eth)). Thanks to Peter Krawitz and Christian Brandt. Williams Syndrome Association
Stefan Barakat Erasmus MC Genetica Erasmus MC WOW! Next level game-changer for these critically ill children. 2 days? what magic is that? We need to talk! RareDiseaseGenomicsRSA - we have so much still to do and what a time to be doing #genomics