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

✍ Scribed by 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. Milhorat; Marcy C. Speer

• Book ID: 101449316
• Publisher: John Wiley and Sons
• Year: 2006
• Tongue: English
• Weight: 201 KB
• Volume: 140A
• Category: Article
• ISSN: 1552-4825
• DOI: 10.1002/ajmg.a.31546