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An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3-Xp21.3.
Ferrero GB, Franco B, Roth EJ, Firulli BA, Borsani G, Delmas-Mata J, Weissenbach J, Halley G, Schlessinger D, Chinault AC, Zoghbi HY, Nelson DL, Ballabio A. Ferrero GB, et al. Among authors: schlessinger d. Hum Mol Genet. 1995 Oct;4(10):1821-7. doi: 10.1093/hmg/4.10.1821. Hum Mol Genet. 1995. PMID: 8595402
A submicroscopic deletion in Xq26 associated with familial situs ambiguus.
Ferrero GB, Gebbia M, Pilia G, Witte D, Peier A, Hopkin RJ, Craigen WJ, Shaffer LG, Schlessinger D, Ballabio A, Casey B. Ferrero GB, et al. Among authors: schlessinger d. Am J Hum Genet. 1997 Aug;61(2):395-401. doi: 10.1086/514857. Am J Hum Genet. 1997. PMID: 9311745 Free PMC article.
X-linked situs abnormalities result from mutations in ZIC3.
Gebbia M, Ferrero GB, Pilia G, Bassi MT, Aylsworth A, Penman-Splitt M, Bird LM, Bamforth JS, Burn J, Schlessinger D, Nelson DL, Casey B. Gebbia M, et al. Among authors: schlessinger d. Nat Genet. 1997 Nov;17(3):305-8. doi: 10.1038/ng1197-305. Nat Genet. 1997. PMID: 9354794
Genome analysis and the human X chromosome.
Mandel JL, Monaco AP, Nelson DL, Schlessinger D, Willard H. Mandel JL, et al. Among authors: schlessinger d. Science. 1992 Oct 2;258(5079):103-9. doi: 10.1126/science.1439756. Science. 1992. PMID: 1439756 Review.
623 results