Homozygosity Mapping in Families with Joubert Syndrome Identifies a Locus on Chromosome 9q34.3 and Evidence for Genetic Heterogeneity  Kathrin Saar, Lihadh.

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Homozygosity Mapping in Families with Joubert Syndrome Identifies a Locus on Chromosome 9q34.3 and Evidence for Genetic Heterogeneity  Kathrin Saar, Lihadh Al-Gazali, László Sztriha, Franz Rueschendorf, Mohammed Nur-E-Kamal, André Reis, Riad Bayoumi  The American Journal of Human Genetics  Volume 65, Issue 6, Pages 1666-1671 (December 1999) DOI: 10.1086/302655 Copyright © 1999 The American Society of Human Genetics Terms and Conditions

Figure 1 Pedigrees and most likely haplotypes for markers on chromosome 9q34 for families A–D. Symbols of affected individuals are blackened. The American Journal of Human Genetics 1999 65, 1666-1671DOI: (10.1086/302655) Copyright © 1999 The American Society of Human Genetics Terms and Conditions

Figure 2 Assignment of markers D9S164, D9S1818, D9S114, D9S1826, D9158, and D9S1838 to the long arm of chromosome 9. Marker distances are taken from Dib et al. (1996). The American Journal of Human Genetics 1999 65, 1666-1671DOI: (10.1086/302655) Copyright © 1999 The American Society of Human Genetics Terms and Conditions

Figure 3 Multipoint analysis performed with Linkmap (from the FASTLINK package version 4.0P) for family A, with the markers D9S1826, D9S158, and D9S1838, resulting in a maximal LOD score of Z=+3.7 at marker D9S158. The American Journal of Human Genetics 1999 65, 1666-1671DOI: (10.1086/302655) Copyright © 1999 The American Society of Human Genetics Terms and Conditions

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