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Bert Callewaert
@CallewaertBert
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Associate professor Ghent University Head of Clinic, Ghent University Hospital Senior Clinical Investigator of the Research Foundation - Flanders
Joined October 2018
RT @HaoYin20: #MyhreSyndrome in Adulthood #SMAD4 N=24 9x R496C 14x I500 variants 1x unknown? Genotype-Phenotype associations 6 with progr…
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Our neighbours have a genetics society for 75 years! Join the special edition meeting and send your abstract in! @HaelstMieke @BeSHGenet
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RT @HaoYin20: An adult (6 mpf) #Zebrafish model of #AorticDissection #AorticRupture (without #AorticAneurysm) Quadriple smad3a/3b/smad6a/6b…
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RT @ClassicFM: Maria João Pires didn’t realise she had prepared the wrong Mozart piano concerto until the orchestra started playing, to a l…
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RT @AJHGNews: 🚨 Online now! 📰Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual dis…
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After a 6 yr long journey, we ended the diagnostic oddysey for many individuals with ZFHX3 loss of function variants. It was a fantastic journey with many international and wonderful colleagues! Great collaboration with @SVergult and @FunGenLab! There's more to come! @AJHGNews
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RT @NatureMedicine: Academic clinician–scientists risk becoming an endangered species. World View from @StephenORahilly @Cambridge_Uni ht…
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RT @MarfanFdn: “This award results from a continuous commitment by MarfanFdn to support research. Being a grantee provides me & my team wit…
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@OdedRechavi Although Gould did it effortless, but public frightened him. He died much too soon...
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RT @MyhreSyndrome: Calling all rare disease researchers, on 14 October, hear from @CallewaertBert and @MarkELindsay, who will be giving upd…
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RT @MyhreSyndrome: For our friends who aren't part of the Myhre family, we've got an extra sprinkle of excitement just for you! 🎉 Introdu…
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RT @uzgent: 🧬 Dermatologen, kinderartsen en klinisch genetici, duik in de wereld van de zeldzame huidziekten met het symposium 'Dermatogene…
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