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Linkage of Tuberculosis to Chromosome 2q35 Loci, Including NRAMP1, in a Large Aboriginal Canadian FamilyCelia M.T. Greenwood, Kenneth Morgan, Takuya Fujiwara et al.|The American Journal of Human Genetics|2000Cited by 203
The most common mutation inFKRP causing limb girdle muscular dystrophy type 2I (LGMD2I) may have occurred only once and is present in Hutterites and other populationsPatrick Frosk, Klaus Wrogemann, Cheryl R. Greenberg et al.|Human Mutation|2004Cited by 77
Hereditary Hypophosphatemic Rickets with Hypercalciuria Is Not Caused by Mutations in the Na/Pi Cotransporter NPT2 GeneA Jones, Harriet S. Tenenhouse, Jordana Tzenova et al.|Journal of the American Society of Nephrology|2001Cited by 70
A locus for Bowen–Conradi syndrome maps to chromosome region 12p13.3Ryan E. Lamont, Teresa Zelinski, Kenneth Morgan et al.|American Journal of Medical Genetics Part A|2004Cited by 14