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Description Phenotypic analysis of patient II-1. A) Panoramic dental X-ray showing hypodontia (arrow 1) and area of maxillary hypoplasia (arrow 2), B: Eye imaging showing polycoria.
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Source de la Houssaye G, Bieche I, Roche O, Vieira V, Laurendeau I, Arbogast L, Zeghidi H, Rapp P, Halimi P, Vidaud M, Dufier JL, Menasche M, Abitbol M. Identification of the first intragenic deletion of the PITX2 gene causing an Axenfeld-Rieger Syndrome: case report. BMC Med Genet. 7, 82. 2006. PMID 17134502. DOI:10.1186/1471-2350-7-82
Author de la Houssaye G et al
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current14:39, 19 November 2007Thumbnail for version as of 14:39, 19 November 2007551 × 853 (109 KB)Filip em (talk | contribs){{Information |Description=Phenotypic analysis of patient II-1. A) Panoramic dental X-ray showing hypodontia (arrow 1) and area of maxillary hypoplasia (arrow 2), B: Eye imaging showing polycoria. |Source=de la Houssaye G, Bieche I, Roche O, Vieira V, Lau

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