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

Abee L. Boyles, David S. Enterline, Preston H. Hammock, Deborah G. Siegel, Susan H. Slifer, Lorraine Mehltretter, John R. Gilbert, Diane Hu-Lince, Dietrich Stephan, Ulrich Batzdorf, Edward Benzel, Richard Ellenbogen, Barth A. Green, Roger Kula, Arnold Menezes, Diane Mueller, John J. Oro, Bermans J. Iskandar, Timothy M. George, Thomas H. MilhoratMarcy C. Speer

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Medicine & Life Sciences