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Phenotypic definition of Chiari type I malformation coupled with high-density SNP genome screen shows significant evidence for linkage to regions on chromosomes 9 and 15.
Boyles AL, Enterline DS, Hammock PH, Siegel DG, Slifer SH, Mehltretter L, Gilbert JR, Hu-Lince D, Stephan D, Batzdorf U, Benzel E, Ellenbogen R, Green BA, Kula R, Menezes A, Mueller D, Oro' JJ, Iskandar BJ, George TM, Milhorat TH, Speer MC. Boyles AL, et al. Among authors: milhorat th. Am J Med Genet A. 2006 Dec 15;140(24):2776-85. doi: 10.1002/ajmg.a.31546. Am J Med Genet A. 2006. PMID: 17103432
"Styloid" syncope.
Chen JX, Kula RW, Bolognese PA, Milhorat TH. Chen JX, et al. Among authors: milhorat th. Neurology. 2008 Nov 11;71(20):1649. doi: 10.1212/01.wnl.0000334762.90440.67. Neurology. 2008. PMID: 19001258 No abstract available.
109 results