Torthaí cuardaigh - Loeys, Bart

Hide and seek: Somatic SMAD3 mutations in melorheostosis de réir Velchev, Joe Davis, Verstraeten, Aline, Loeys, Bart

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Educational paper: Connective tissue disorders with vascular involvement: from gene to therapy de réir Van Laer, Lut, Proost, Dorien, Loeys, Bart L.

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Generation of two induced pluripotent stem cell (iPSC) lines (BBANTWi006-A, BBANTWi007-A) from Brugada syndrome patients carrying an SCN5A mutation de réir Simons, Eline, Nijak, Aleksandra, Loeys, Bart, Alaerts, Maaike

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Preventing the aortic complications of Marfan syndrome: a case-example of translational genomic medicine de réir Li-Wan-Po, Alain, Loeys, Bart, Farndon, Peter, Latham, David, Bradley, Caroline

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The diagnostic value of the facial features of Marfan syndrome de réir Ting, Beverlie L., Mathur, Deepti, Loeys, Bart L., Dietz, Harry C., Sponseller, Paul D.

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VariantDB: a flexible annotation and filtering portal for next generation sequencing data de réir Vandeweyer, Geert, Van Laer, Lut, Loeys, Bart, Van den Bulcke, Tim, Kooy, R Frank

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iPSC-Cardiomyocyte Models of Brugada Syndrome—Achievements, Challenges and Future Perspectives de réir Nijak, Aleksandra, Saenen, Johan, Labro, Alain J., Schepers, Dorien, Loeys, Bart L., Alaerts, Maaike

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The fibrillinopathies: New insights with focus on the paradigm of opposing phenotypes for both FBN1 and FBN2 de réir Peeters, Silke, De Kinderen, Pauline, Meester, Josephina A. N., Verstraeten, Aline, Loeys, Bart L.

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Angiotensin II Blockade and Aortic-Root Dilation in Marfan’s Syndrome de réir Brooke, Benjamin S., Habashi, Jennifer P., Judge, Daniel P., Patel, Nishant, Loeys, Bart, Dietz, Harry C.

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Biglycan in the Skeleton de réir Kram, Vardit, Shainer, Reut, Jani, Priyam, Meester, Josephina A.N., Loeys, Bart, Young, Marian F.

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Clinical utility gene card for: Loeys-Dietz syndrome (TGFBR1/2) and related phenotypes de réir Arslan-Kirchner, Mine, Epplen, Jörg T, Faivre, Laurence, Jondeau, Guillaume, Schmidtke, Jörg, De Paepe, Anne, Loeys, Bart

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Differences in manifestations of Marfan syndrome, Ehlers-Danlos syndrome, and Loeys-Dietz syndrome de réir Meester, Josephina A. N., Verstraeten, Aline, Schepers, Dorien, Alaerts, Maaike, Van Laer, Lut, Loeys, Bart L.

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Intermittent Brugada syndrome in an anorexic adolescent girl de réir Docx, Martine K.F., Loeys, Bart, Simons, Annik, Gewillig, Marc, Proost, Dorien, Van Laer, Lut, Mertens, Luc

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pBRIT: gene prioritization by correlating functional and phenotypic annotations through integrative data fusion de réir Kumar, Ajay Anand, Van Laer, Lut, Alaerts, Maaike, Ardeshirdavani, Amin, Moreau, Yves, Laukens, Kris, Loeys, Bart, Vandeweyer, Geert

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Identification of FBN1 gene mutations in Ukrainian Marfan syndrome patients de réir ZHURAYEV, RUSTAM, PROOST, DORIEN, ZERBINO, DMYTRO, FEDORENKO, VIKTOR, MEESTER, JOSEPHINA A. N., VAN LAER, LUT, LOEYS, BART L.

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Nasal speech and hypothyroidism are common hallmarks of 12q15 microdeletions de réir Vergult, Sarah, Krgovic, Danijela, Loeys, Bart, Lyonnet, Stanislas, Liedén, Agne, Anderlid, Britt-Marie, Sharkey, Freddie, Joss, Shelagh, Mortier, Geert, Menten, Björn

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Nasal speech in patients with 12q15 microdeletions de réir Vergult, Sarah, Krgovic, Danijela, Loeys, Bart, Lyonnet, Stanislas, Liedén, Agne, Anderlid, Britt-Marie, Sharkey, Freddie, Joss, Shelagh, Mortier, Geert, Menten, Björn

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FLNA mutations in surviving males presenting with connective tissue findings: two new case reports and review of the literature de réir Cannaerts, Elyssa, Shukla, Anju, Hasanhodzic, Mensuda, Alaerts, Maaike, Schepers, Dorien, Van Laer, Lut, Girisha, Katta M., Hojsak, Iva, Loeys, Bart, Verstraeten, Aline

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Clinical utility gene card for: Marfan syndrome type 1 and related phenotypes [FBN1] de réir Arslan-Kirchner, Mine, Arbustini, Eloisa, Boileau, Catherine, Child, Anne, Collod-Beroud, Gwenaelle, De Paepe, Anne, Epplen, Jörg, Jondeau, Guillaume, Loeys, Bart, Faivre, Laurence

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First evidence of maternally inherited mosaicism in TGFBR1 and subtle primary myocardial changes in Loeys-Dietz syndrome: a case report de réir Baban, Anwar, Magliozzi, Monia, Loeys, Bart, Adorisio, Rachele, Alesi, Viola, Secinaro, Aurelio, Corica, Bernadette, Vricella, Luca, Dietz, Harry C., Drago, Fabrizio, Novelli, Antonio, Amodeo, Antonio

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