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Author/Creator Devriendt, Koen

12. Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3. (October 2017)

Authors:
Guo, Tingwei; Repetto, Gabriela M.; McDonald McGinn, Donna M.; Chung, Jonathan H.; Nomaru, Hiroko; Campbell, Christopher L.; Blonska, Anna; Bassett, Anne S.; Chow, Eva W.C.; Mlynarski, Elisabeth E.; Swillen, Ann; Vermeesch, Joris; Devriendt, Koen; Gothelf, Doron; Carmel, Miri; Michaelovsky, Elena...
Journal:
Circulation
Issue:
Volume 10:Number 5(2017)
Page Start:
Record Type:
Journal Article
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13. Genomic rearrangements of the GREM1-FMN1 locus cause oligosyndactyly, radio-ulnar synostosis, hearing loss, renal defects syndrome and Cenani–Lenz-like non-syndromic oligosyndactyly. Issue 8 (7th July 2010)

Authors:
Dimitrov, Boyan Ivanov; Voet, Thierry; De Smet, Luc; Vermeesch, Joris Robert; Devriendt, Koen; Fryns, Jean-Pierre; Debeer, Philippe
Journal:
Journal of medical genetics
Issue:
Volume 47:Issue 8(2010)
Page Start:
569
Record Type:
Journal Article
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16. Metal mining and birth defects: a case-control study in Lubumbashi, Democratic Republic of the Congo. Issue 4 (April 2020)

Authors:
Van Brusselen, Daan; Kayembe-Kitenge, Tony; Mbuyi-Musanzayi, Sébastien; Lubala Kasole, Toni; Kabamba Ngombe, Leon; Musa Obadia, Paul; Kyanika wa Mukoma, Daniel; Van Herck, Koen; Avonts, Dirk; Devriendt, Koen; Smolders, Erik; Nkulu, Célestin Banza Lubaba; Nemery, Benoit
Journal:
Lancet
Issue:
Volume 4:Issue 4(2020)
Page Start:
e158
Record Type:
Journal Article
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18. Molecular screening of ADAMTSL2 gene in 33 patients reveals the genetic heterogeneity of geleophysic dysplasia. Issue 6 (17th March 2011)

Authors:
Allali, Slimane; Le Goff, Carine; Pressac–Diebold, Isabelle; Pfennig, Gwendoline; Mahaut, Clémentine; Dagoneau, Nathalie; Alanay, Yasemin; Brady, Angela F; Crow, Yanick J; Devriendt, Koen; Drouin-Garraud, Valérie; Flori, Elisabeth; Geneviève, David; Hennekam, Raoul C; Hurst, Jane; Krakow, Deborah...
Journal:
Journal of medical genetics
Issue:
Volume 48:Issue 6(2011)
Page Start:
417
Record Type:
Journal Article
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19. Non‐invasive prenatal testing suggesting a maternal malignancy: What do we tell the prospective parents in Belgium?. (26th August 2021)

Authors:
Lannoo, Lore; Lenaerts, Liesbeth; Van Den Bogaert, Kris; Che, Huiwen; Brison, Nathalie; Devriendt, Koen; Amant, Frédéric; Vermeesch, Joris Robert; Van Calsteren, Kristel
Journal:
Prenatal diagnosis
Issue:
Volume 41:Number 10(2021)
Page Start:
1264
Record Type:
Journal Article
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20. Olfactory function in patients with nonsyndromic orofacial clefts and their unaffected relatives. Issue 11 (22nd October 2018)

Authors:
Roosenboom, Jasmien; Hermans, Robert; Lammens, Frederik; Samain, Jean Louis; Devriendt, Koen; Vander Poorten, Vincent; Hellings, Peter W.; Jorissen, Mark; Peeters, Hilde; Claes, Peter; Hens, Greet
Journal:
American journal of medical genetics
Issue:
Volume 176:Issue 11(2018)
Page Start:
2375
Record Type:
Journal Article
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