Full text
PDF
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Ben Othmane K., Ben Hamida M., Pericak-Vance M. A., Ben Hamida C., Blel S., Carter S. C., Bowcock A. M., Petruhkin K., Gilliam T. C., Roses A. D. Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q. Nat Genet. 1992 Dec;2(4):315–317. doi: 10.1038/ng1292-315. [DOI] [PubMed] [Google Scholar]
- Ben Othmane K., Hentati F., Lennon F., Ben Hamida C., Blel S., Roses A. D., Pericak-Vance M. A., Ben Hamida M., Vance J. M. Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q. Hum Mol Genet. 1993 Oct;2(10):1625–1628. doi: 10.1093/hmg/2.10.1625. [DOI] [PubMed] [Google Scholar]
- Ben Othmane K., Middleton L. T., Loprest L. J., Wilkinson K. M., Lennon F., Rozear M. P., Stajich J. M., Gaskell P. C., Roses A. D., Pericak-Vance M. A. Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity. Genomics. 1993 Aug;17(2):370–375. doi: 10.1006/geno.1993.1334. [DOI] [PubMed] [Google Scholar]
- Cottingham R. W., Jr, Idury R. M., Schäffer A. A. Faster sequential genetic linkage computations. Am J Hum Genet. 1993 Jul;53(1):252–263. [PMC free article] [PubMed] [Google Scholar]
- Fischbeck K. H., ar-Rushdi N., Pericak-Vance M., Rozear M., Roses A. D., Fryns J. P. X-linked neuropathy: gene localization with DNA probes. Ann Neurol. 1986 Oct;20(4):527–532. doi: 10.1002/ana.410200414. [DOI] [PubMed] [Google Scholar]
- Knowles J. A., Vieland V. J., Gilliam T. C. Perils of gene mapping with microsatellite markers. Am J Hum Genet. 1992 Oct;51(4):905–909. [PMC free article] [PubMed] [Google Scholar]
- Kwon J. M., Elliott J. L., Yee W. C., Ivanovich J., Scavarda N. J., Moolsintong P. J., Goodfellow P. J. Assignment of a second Charcot-Marie-Tooth type II locus to chromosome 3q. Am J Hum Genet. 1995 Oct;57(4):853–858. [PMC free article] [PubMed] [Google Scholar]
- Loprest L. J., Pericak-Vance M. A., Stajich J., Gaskell P. C., Lucas A. M., Lennon F., Yamaoka L. H., Roses A. D., Vance J. M. Linkage studies in Charcot-Marie-Tooth disease type 2: evidence that CMT types 1 and 2 are distinct genetic entities. Neurology. 1992 Mar;42(3 Pt 1):597–601. doi: 10.1212/wnl.42.3.597. [DOI] [PubMed] [Google Scholar]
- Rozear M. P., Pericak-Vance M. A., Fischbeck K., Stajich J. M., Gaskell P. C., Jr, Krendel D. A., Graham D. G., Dawson D. V., Roses A. D. Hereditary motor and sensory neuropathy, X-linked: a half century follow-up. Neurology. 1987 Sep;37(9):1460–1465. doi: 10.1212/wnl.37.9.1460. [DOI] [PubMed] [Google Scholar]
- Schäffer A. A., Gupta S. K., Shriram K., Cottingham R. W., Jr Avoiding recomputation in linkage analysis. Hum Hered. 1994 Jul-Aug;44(4):225–237. doi: 10.1159/000154222. [DOI] [PubMed] [Google Scholar]
- Vance J. M., Barker D., Yamaoka L. H., Stajich J. M., Loprest L., Hung W. Y., Fischbeck K., Roses A. D., Pericak-Vance M. A. Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2. Genomics. 1991 Apr;9(4):623–628. doi: 10.1016/0888-7543(91)90355-i. [DOI] [PubMed] [Google Scholar]
- Vance J. M., Nicholson G. A., Yamaoka L. H., Stajich J., Stewart C. S., Speer M. C., Hung W. Y., Roses A. D., Barker D., Pericak-Vance M. A. Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17. Exp Neurol. 1989 May;104(2):186–189. doi: 10.1016/s0014-4886(89)80013-5. [DOI] [PubMed] [Google Scholar]