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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
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, RicVolume:
140A
Year:
2006
Language:
english
Pages:
10
DOI:
10.1002/ajmg.a.31546
File:
PDF, 201 KB
english, 2006