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Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population.

Bibliographic reference Ghassibé, Michella ; Bayet, Benedicte ; Revencu, Nicole ; Dumoulin, Christine ; Gillerot, Yves ; et. al. Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population.. In: European journal of human genetics : EJHG, Vol. 13, no. 11, p. 1239-42 (2005)
Permanent URL http://hdl.handle.net/2078.1/21951
  1. Murray Jeffrey C., Schutte Brian C., Cleft palate: players, pathways, and pursuits, 10.1172/jci200422154
  2. van den Boogaard Marie-José H., Dorland Marinus, Beemer Frits A., van Amstel Hans Kristian Ploos, 10.1038/74155
  3. FitzPatrick D. R., Identification of SATB2 as the cleft palate gene on 2q32-q33, 10.1093/hmg/ddg248
  4. Loeys Bart L, Chen Junji, Neptune Enid R, Judge Daniel P, Podowski Megan, Holm Tammy, Meyers Jennifer, Leitch Carmen C, Katsanis Nicholas, Sharifi Neda, Xu F Lauren, Myers Loretha A, Spevak Philip J, Cameron Duke E, Backer Julie De, Hellemans Jan, Chen Yan, Davis Elaine C, Webb Catherine L, Kress Wolfram, Coucke Paul, Rifkin Daniel B, De Paepe Anne M, Dietz Harry C, A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2, 10.1038/ng1511
  5. Murray JC, Gene/environment causes of cleft lip and/or palate : Gene/environment causes of cleft lip and palate, 10.1034/j.1399-0004.2002.610402.x
  6. Jones MC, Cleft Palate J, 25, 16 (1988)
  7. Schutte B. C., The many faces and factors oforofacial clefts, 10.1093/hmg/8.10.1853
  8. Van der Woude A, Am J Hum Genet, 6, 244 (1954)
  9. Lacombe D, Genet Counsel, 6, 221 (1995)
  10. Houdayer C, Ann Genet, 42, 69 (1999)
  11. Kondo Shinji, Schutte Brian C., Richardson Rebecca J., Bjork Bryan C., Knight Alexandra S., Watanabe Yoriko, Howard Emma, Ferreira de Lima Renata L.L., Daack-Hirsch Sandra, Sander Achim, McDonald-McGinn Donna M., Zackai Elaine H., Lammer Edward J., Aylsworth Arthur S., Ardinger Holly H., Lidral Andrew C., Pober Barbara R., Moreno Lina, Arcos-Burgos Mauricio, Valencia Consuelo, Houdayer Claude, Bahuau Michel, Moretti-Ferreira Danilo, Richieri-Costa Antonio, Dixon Michael J., Murray Jeffrey C., Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes, 10.1038/ng985
  12. Ghassibe M, Six families with van der Woude and/or popliteal pterygium syndrome: all with a mutation in the IRF6 gene, 10.1136/jmg.2003.009274
  13. Zucchero Theresa M., Cooper Margaret E., Maher Brion S., Daack-Hirsch Sandra, Nepomuceno Buena, Ribeiro Lucilene, Caprau Diana, Christensen Kaare, Suzuki Yasushi, Machida Junichiro, Natsume Nagato, Yoshiura Koh-Ichiro, Vieira Alexandre R., Orioli Ieda M., Castilla Eduardo E., Moreno Lina, Arcos-Burgos Mauricio, Lidral Andrew C., Field L. Leigh, Liu You-e, Ray Ajit, Goldstein Toby H., Schultz Rebecca E., Shi Min, Johnson Marla K., Kondo Shinji, Schutte Brian C., Marazita Mary L., Murray Jeffrey C., Interferon Regulatory Factor 6 (IRF6) Gene Variants and the Risk of Isolated Cleft Lip or Palate, 10.1056/nejmoa032909
  14. Scapoli Luca, Palmieri Annalisa, Martinelli Marcella, Pezzetti Furio, Carinci Paolo, Tognon Mauro, Carinci Francesco, Strong Evidence of Linkage Disequilibrium between Polymorphisms at the IRF6 Locus and Nonsyndromic Cleft Lip With or Without Cleft Palate, in an Italian Population, 10.1086/427344
  15. Spielman RS, Am J Hum Genet, 52, 506 (1993)
  16. Daly MJ, Kruglyak L & Pratt S et al. Genehunter Documentation, version 2.0 beta 1998; http://linkage.rockefeller.edu/soft/gh/index.html.
  17. Horvath Steve, Xu Xin, Laird Nan M, The family based association test method: strategies for studying general genotype–phenotype associations, 10.1038/sj.ejhg.5200625
  18. Laird Nan M., Horvath Steve, Xu Xin, Implementing a unified approach to family-based tests of association, 10.1002/1098-2272(2000)19:1+<::aid-gepi6>3.0.co;2-m
  19. Access to FBAT and HaploFBAT at http://www.biostat.harvard.edu/~fbat/default.html.
  20. Abecasis G. R., Cookson W. O. C., GOLD--Graphical Overview of Linkage Disequilibrium, 10.1093/bioinformatics/16.2.182
  21. Stanier P., Forbes S.A., Arnason A., Bjornsson A., Sveinbjornsdottir E., Williamson R., Moore G., The Localization of a Gene Causing X-Linked Cleft Palate and Ankyloglossia (CPX) in an Icelandic Kindred Is between DXS326 and DXYS1X, 10.1006/geno.1993.1370
  22. van den Boogaard Marie-José H., Dorland Marinus, Beemer Frits A., van Amstel Hans Kristian Ploos, 10.1038/74155
  23. Celli Jacopo, Duijf Pascal, Hamel Ben C.J, Bamshad Michael, Kramer Bridget, Smits Arie P.T, Newbury-Ecob Ruth, Hennekam Raoul C.M, Van Buggenhout Griet, van Haeringen Arie, Woods C.Geoffrey, van Essen Anthonie J, de Waal Rob, Vriend Gert, Haber Daniel A, Yang Annie, McKeon Frank, Brunner Han G, van Bokhoven Hans, Heterozygous Germline Mutations in the p53 Homolog p63 Are the Cause of EEC Syndrome, 10.1016/s0092-8674(00)81646-3
  24. Dodé Catherine, Levilliers Jacqueline, Dupont Jean-Michel, De Paepe Anne, Le Dû Nathalie, Soussi-Yanicostas Nadia, Coimbra Roney S., Delmaghani Sedigheh, Compain-Nouaille Sylvie, Baverel Françoise, Pêcheux Christophe, Le Tessier Dominique, Cruaud Corinne, Delpech Marc, Speleman Frank, Vermeulen Stefan, Amalfitano Andrea, Bachelot Yvan, Bouchard Philippe, Cabrol Sylvie, Carel Jean-Claude, Delemarre-van de Waal Henriette, Goulet-Salmon Barbara, Kottler Marie-Laure, Richard Odile, Sanchez-Franco Franco, Saura Robert, Young Jacques, Petit Christine, Hardelin Jean-Pierre, Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome, 10.1038/ng1122
  25. Loeys Bart L, Chen Junji, Neptune Enid R, Judge Daniel P, Podowski Megan, Holm Tammy, Meyers Jennifer, Leitch Carmen C, Katsanis Nicholas, Sharifi Neda, Xu F Lauren, Myers Loretha A, Spevak Philip J, Cameron Duke E, Backer Julie De, Hellemans Jan, Chen Yan, Davis Elaine C, Webb Catherine L, Kress Wolfram, Coucke Paul, Rifkin Daniel B, De Paepe Anne M, Dietz Harry C, A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2, 10.1038/ng1511