Identification of the first intragenic deletion of the PITX2 gene causing an Axenfeld-Rieger Syndrome: case report.
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.
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BMC Med Genet. 2006 Nov 29;7:82. doi: 10.1186/1471-2350-7-82.
BMC Med Genet. 2006.
PMID: 17134502
Free PMC article.