Linkage Analysis in a Large Brazilian Family with van der Woude Syndrome Suggests the Existence of a Susceptibility Locus for Cleft Palate at 17p11.2-11.1

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Linkage Analysis in a Large Brazilian Family with van der Woude Syndrome Suggests the Existence of a Susceptibility Locus for Cleft Palate at 17p11.2-11.1 Andréa L. Sertié, Andreza V. Sousa, Silvio Steman, Rita C. Pavanello, M. Rita Passos-Bueno The American Journal of Human Genetics Volume 65, Issue 2, Pages 433-440 (August 1999) DOI: 10.1086/302491 Copyright © 1999 The American Society of Human Genetics Terms and Conditions

Figure 1 Haplotype analysis for the most informative markers from the 1q32-41 region, that showed linkage to the VWS gene. Only the individuals who were available for DNA studies were included. The at-risk haplotype for VWS is boxed. The American Journal of Human Genetics 1999 65, 433-440DOI: (10.1086/302491) Copyright © 1999 The American Society of Human Genetics Terms and Conditions

Figure 2 A, Haplotype with markers from the 17p11.2-11.1 region in the sibship III-1–III-16. The at-risk haplotype for the CP-predisposing locus in the family is boxed. The order and interlocus distances among the markers are from the Généthon map (Dib et al. 1996). Only individuals with CP, independently of the presence of other clinical features of VWS, are indicated as affected (blackened circles). B, Haplotype with the most informative markers from the 17p11.2-11.1 region, in the total family. The at-risk haplotype for the CP-predisposing locus in the family is boxed. Only individuals with CP, independently of the presence of other clinical features of VWS, are indicated as affected (blackened circles). The American Journal of Human Genetics 1999 65, 433-440DOI: (10.1086/302491) Copyright © 1999 The American Society of Human Genetics Terms and Conditions