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Top Tweets for #opitzC

GeneticsUB's profile image
GeneticsUB @GeneticsUB
Today is #RareDiseaseDay. @GeneticsUB many research labs are working in #RareDiseases. From #OpitzC to #Retinitispigmentosa to #SCAN1, different approaches to better understand #RareDisease from #genetics to possible future treatments
GeneticsUB's tweet photo. Today is #RareDiseaseDay. @GeneticsUB many research labs are working in #RareDiseases. From #OpitzC to #Retinitispigmentosa to #SCAN1, different approaches to better understand #RareDisease from #genetics to possible future treatments https://t.co/9kUhwGI1Rv
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NoInvisibles's profile image
RarasNoInvisibles Verified account @NoInvisibles
Síndrome de #OpitzC: nuevos avances para mejorar el diagnóstico genético de esta enfermedad ultrarrara W Síndrome Smith-Lemli-Opitz En @FEMEXER de @mgenomica Cc @Roser_uf @CIBERER @UniBarcelona https://t.co/BEGAEEcdxX
NoInvisibles's tweet photo. Síndrome de #OpitzC: nuevos avances para mejorar el diagnóstico genético de esta enfermedad ultrarrara W Síndrome Smith-Lemli-Opitz En @FEMEXER de @mgenomica Cc @Roser_uf @CIBERER @UniBarcelona https://t.co/BEGAEEcdxX https://t.co/gGwfx8S481
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PilulariAnimans's profile image
Pilularia @PilulariAnimans
Un Benelux poco frecuente. #EnfermedadesRaras #Rare Diseases #EERR #Wolfram #SturgeWeber #OpitzC #SaludPublica #investigación #pocofrecuentes #minoritarias https://t.co/XCmCBMZQHx
PilulariAnimans's tweet photo. Un Benelux poco frecuente. #EnfermedadesRaras #Rare Diseases #EERR #Wolfram #SturgeWeber #OpitzC #SaludPublica #investigación #pocofrecuentes #minoritarias https://t.co/XCmCBMZQHx https://t.co/uhB3sqjGV8
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Roser_uf's profile image
Dra. Roser Urreizti @Roser_uf
Gracias a estas ayudas, al papel de los ciudadanos, de los pacientes y de sus familias, podemos seguir avanzando en la investigación🔬 de las enfermedades más minoritarias, como #SchaafYang, #OpitzC, #FOXP1 y otras con apenas unas decenas de afectados en todo el 🌍 ¡GRACIAS! ❤️ https://t.co/fTPx9D2d3I
SindromeOpitzC's profile image
Síndrome Opitz C @SindromeOpitzC
Nuestra asociación ha destinado los 32.000 euros de esta ayuda íntegramente a la investigación genética para la búsqueda de terapias que desarrolla el equipo de Genética Humana de la @UniBarcelona @Roser_uf @NoInvisibles @FEDER_ONG @xavigranda https://t.co/YaMz0DQt2W
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PCB_UB's profile image
Parc Científic de Barcelona @PCB_UB
Researchers from #IBUB at @PCB_UB find gene causing #OpitzC syndrome in the only patient in Catalonia https://t.co/FS7lrdc7FA #PCBCommunity
PCB_UB's tweet photo. Researchers from #IBUB at @PCB_UB find gene causing #OpitzC syndrome in the only patient in Catalonia https://t.co/FS7lrdc7FA #PCBCommunity https://t.co/3cVclb09yi
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NoInvisibles's profile image
RarasNoInvisibles Verified account @NoInvisibles
Exito d la investigación 👏🏻 Anuncia @CIBERER Identifican gen causante del Sind. d #OpitzC Raro pero no invisible https://t.co/wi550jNAW6 2/2
NoInvisibles's tweet photo. Exito d la investigación 👏🏻 Anuncia @CIBERER Identifican gen causante del Sind. d #OpitzC Raro pero no invisible https://t.co/wi550jNAW6 2/2 https://t.co/FWAGJrdRef
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FECYT_Ciencia's profile image
FECYT @FECYT_Ciencia
Investigadores de un proyecto exitoso de @precipitamos encuentran el #gen causante del Síndrome de #OpitzC https://t.co/EwqAsscTkm
FECYT_Ciencia's tweet photo. Investigadores de un proyecto exitoso de @precipitamos encuentran el #gen causante del Síndrome de #OpitzC https://t.co/EwqAsscTkm https://t.co/9Q5Sisdbsq
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Ar_1News's profile image
AR NEWS @Ar_1News
Identificado Gene que causa desordem rara,a Síndrome de Opitz C https://t.co/7Cqe6wvsVY #MedicalArticle #OpitzC
Ar_1News's tweet photo. Identificado Gene que causa desordem rara,a Síndrome de Opitz C https://t.co/7Cqe6wvsVY #MedicalArticle #OpitzC https://t.co/7vUZYUWygs
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milycimadevilla's profile image
mily cimadevilla @milycimadevilla
· Noreña
La tele de los asturian@s @TPAnoticias adelantó el viernes pasado esta #investigacion financiada con #micromecenazgo #opitzC #ciencia https://t.co/Z7H4TILCX7
ConSalud_es's profile image
ConSalud.es Verified account @ConSalud_es
Encuentran el origen del síndrome de Opitz C, una patología ultrarrara que solo afecta a 3 personas en España https://t.co/28qLBdU1OI
ConSalud_es's tweet photo. Encuentran el origen del síndrome de Opitz C, una patología ultrarrara que solo afecta a 3 personas en España https://t.co/28qLBdU1OI https://t.co/484WKXKPVS
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Genetics_LR's profile image
Labroots Genetics & Genomics @Genetics_LR
#Crowdfunding produces discovery - #MAGEL2 #mutation implicated as a #genetic cause of #ultrarare #OpitzC #syndrome https://t.co/OdTlbc3scS
Genetics_LR's tweet photo. #Crowdfunding produces discovery - #MAGEL2 #mutation implicated as a #genetic cause of #ultrarare #OpitzC #syndrome https://t.co/OdTlbc3scS https://t.co/n8ZyMOpge7
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HealthandMed_LR's profile image
Labroots Health & Medicine @HealthandMed_LR
#Crowdfunding produces discovery - #MAGEL2 #mutation implicated as a #genetic cause of #ultrarare #OpitzC #syndrome https://t.co/O9tNMPLUwp
HealthandMed_LR's tweet photo. #Crowdfunding produces discovery - #MAGEL2 #mutation implicated as a #genetic cause of #ultrarare #OpitzC #syndrome https://t.co/O9tNMPLUwp https://t.co/0cyeW8aTYY
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milycimadevilla's profile image
mily cimadevilla @milycimadevilla
Enhorabuena @Roser_uf Investigadores catalanes identifican la mutación que causa #OpitzC por @TPAnoticias https://t.co/jrSITwTlIK https://t.co/oL6F4SkJVW
Roser_uf's profile image
Dra. Roser Urreizti @Roser_uf
#OpitzC & #SchaafYang Syndromes This is the results of a great collaboration: @UniBarcelona @CRGenomica @vallhebron https://t.co/6967wjhnzw
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Roser_uf's profile image
Dra. Roser Urreizti @Roser_uf
#OpitzC & #SchaafYang Syndromes This is the results of a great collaboration: @UniBarcelona @CRGenomica @vallhebron https://t.co/6967wjhnzw
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Roser_uf's profile image
Dra. Roser Urreizti @Roser_uf
Entrega del Xec de @CXinfo per la @SindromeOpitzC per la #recerca en #OpitzC. Nou projecte: https://t.co/a8qprHmtC2
Roser_uf's tweet photo. Entrega del Xec de @CXinfo per la @SindromeOpitzC per la #recerca en #OpitzC. Nou projecte: https://t.co/a8qprHmtC2 https://t.co/4MXmFph9m1
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childrenwithbos's profile image
BohringOpitzSyndrome @childrenwithbos
Wish u, @Roser_uf a succeeded presentation https://t.co/baOLIfHF9q on #OpitzC & #BohringOpitz tomorrow at #ESHG2016
childrenwithbos's tweet photo. Wish u, @Roser_uf a succeeded presentation https://t.co/baOLIfHF9q on #OpitzC & #BohringOpitz tomorrow at #ESHG2016 https://t.co/FbCAMVvn2f
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childrenwithbos's profile image
BohringOpitzSyndrome @childrenwithbos
Looking forward to hear more about your results on #OpitzC and #BohringOpitz! Wish u the best with the presentation! https://t.co/LEmaXFW4eE
Roser_uf's profile image
Dra. Roser Urreizti @Roser_uf
Next Saturday we will be presenting our results on #OpitzC and #BOS at the #ESHG2016 @talynnsjourney @childrenwithbos #RareDisease
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Roser_uf's profile image
Dra. Roser Urreizti @Roser_uf
Next Saturday we will be presenting our results on #OpitzC and #BOS at the #ESHG2016 @talynnsjourney @childrenwithbos #RareDisease
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Roser_uf's profile image
Dra. Roser Urreizti @Roser_uf
Today is #BOSAwarenessDay. Our #5forBos ! I'll be giving a talk about #OpitzC and #BOS today at @HospitalSantPau
Roser_uf's tweet photo. Today is #BOSAwarenessDay. Our #5forBos ! I'll be giving a talk about #OpitzC and #BOS today at @HospitalSantPau https://t.co/xhD4VrdJ1Q
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milycimadevilla's profile image
mily cimadevilla @milycimadevilla
Un gen de una adolescente asturiana puede ayudar a una investigación única en el mundo sobre el sindrome #OpitzC http://t.co/Y535qB39kE
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NoInvisibles's profile image
RarasNoInvisibles Verified account @NoInvisibles
Investigación y financiación del Síndrome d #OpitzC #SLOS En #RPNI "Carrera contra reloj" http://t.co/AIdfdTBAPA
NoInvisibles's tweet photo. Investigación y financiación del Síndrome d #OpitzC #SLOS En #RPNI "Carrera contra reloj" http://t.co/AIdfdTBAPA http://t.co/M3ndvYSZ7w
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