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Genomics|November 26, 1998
Use of a CEPH meiotic breakpoint panel to refine the locus of limb-girdle muscular dystrophy type 1A (LGMD1A) to a 2-Mb interval on 5q31L Bartoloni, S K Horrigan, K D Viles, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 1, 1997
Value of molecular monitoring during the treatment of chronic myeloid leukemia: a Cancer and Leukemia Group B studyW Stock, C A Westbrook, B Peterson, et al.Neuromuscular Disorders : NMD|September 1, 1994
Development of a microsatellite genetic map spanning 5q31-q33 and subsequent placement of the LGMD1A locus between D5S178 and IL9L H Yamaoka, C A Westbrook, M C Speer, et al.Human Heredity|August 7, 1998
Exclusion of identified LGMD1 loci from four dominant limb-girdle muscular dystrophy familiesM C Speer, J M Vance, F Lennon-Graham, et al.Human Molecular Genetics|August 25, 2000
Myotilin is mutated in limb girdle muscular dystrophy 1AM A Hauser, S K Horrigan, P Salmikangas, et al.Pageof 8