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Multilocus mapping of the X-linked hypophosphatemic rickets gene.
Econs MJ, Barker DF, Speer MC, Pericak-Vance MA, Fain PR, Drezner MK. Econs MJ, et al. Among authors: speer mc. J Clin Endocrinol Metab. 1992 Jul;75(1):201-6. doi: 10.1210/jcem.75.1.1352307. J Clin Endocrinol Metab. 1992. PMID: 1352307
A PHEX gene mutation is responsible for adult-onset vitamin D-resistant hypophosphatemic osteomalacia: evidence that the disorder is not a distinct entity from X-linked hypophosphatemic rickets.
Econs MJ, Friedman NE, Rowe PS, Speer MC, Francis F, Strom TM, Oudet C, Smith JA, Ninomiya JT, Lee BE, Bergen H. Econs MJ, et al. Among authors: speer mc. J Clin Endocrinol Metab. 1998 Oct;83(10):3459-62. doi: 10.1210/jcem.83.10.5167. J Clin Endocrinol Metab. 1998. PMID: 9768646
Dinucleotide repeat polymorphism at the DXS1683 locus.
Econs MJ, Francis F, Rowe PS, Speer MC, O'Riordan JL, Lehrach H, Becker PA. Econs MJ, et al. Among authors: speer mc. Hum Mol Genet. 1994 Apr;3(4):680. doi: 10.1093/hmg/3.4.680. Hum Mol Genet. 1994. PMID: 8069326 No abstract available.
Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17.
Vance JM, Nicholson GA, Yamaoka LH, Stajich J, Stewart CS, Speer MC, Hung WY, Roses AD, Barker D, Pericak-Vance MA. Vance JM, et al. Among authors: speer mc. Exp Neurol. 1989 May;104(2):186-9. doi: 10.1016/s0014-4886(89)80013-5. Exp Neurol. 1989. PMID: 2707366
Heterogeneity in Paget disease of the bone.
Nance MA, Nuttall FQ, Econs MJ, Lyles KW, Viles KD, Vance JM, Pericak-Vance MA, Speer MC. Nance MA, et al. Among authors: speer mc. Am J Med Genet. 2000 Jun 19;92(5):303-7. doi: 10.1002/1096-8628(20000619)92:5<303::aid-ajmg2>3.0.co;2-e. Am J Med Genet. 2000. PMID: 10861657
153 results