Smith B - Search Results

1

Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A.

Matsunami N, Smith B, Ballard L, Lensch MW, Robertson M, Albertsen H, Hanemann CO, Müller HW, Bird TD, White R, et al. Matsunami N, et al. Among authors: smith b. Nat Genet. 1992 Jun;1(3):176-9. doi: 10.1038/ng0692-176. Nat Genet. 1992. PMID: 1303231

2

Analysis of the DNA duplication 17p11.2 in Charcot-Marie-Tooth neuropathy type 1 pedigrees: additional evidence for a third autosomal CMT1 locus.

Chance PF, Matsunami N, Lensch W, Smith B, Bird TD. Chance PF, et al. Among authors: smith b. Neurology. 1992 Oct;42(10):2037-41. doi: 10.1212/wnl.42.10.2037. Neurology. 1992. PMID: 1407588

3

DNA deletion associated with hereditary neuropathy with liability to pressure palsies.

Chance PF, Alderson MK, Leppig KA, Lensch MW, Matsunami N, Smith B, Swanson PD, Odelberg SJ, Disteche CM, Bird TD. Chance PF, et al. Among authors: smith b. Cell. 1993 Jan 15;72(1):143-51. doi: 10.1016/0092-8674(93)90058-x. Cell. 1993. PMID: 8422677

4

Deletion of genes on chromosome 1 in endocrine neoplasia.

Mathew CG, Smith BA, Thorpe K, Wong Z, Royle NJ, Jeffreys AJ, Ponder BA. Mathew CG, et al. Among authors: smith ba. Nature. 1987 Aug 6-12;328(6130):524-6. doi: 10.1038/328524a0. Nature. 1987. PMID: 3614355

5

Isolation of DNA markers in the direction of the Huntington disease gene from the G8 locus.

Smith B, Skarecky D, Bengtsson U, Magenis RE, Carpenter N, Wasmuth JJ. Smith B, et al. Am J Hum Genet. 1988 Feb;42(2):335-44. Am J Hum Genet. 1988. PMID: 2963539 Free PMC article.

6

Regional localization of polymorphic markers on chromosome 10 by physical and genetic mapping.

Mathew CG, Wakeling W, Jones E, Easton D, Fisher R, Strong C, Smith B, Chin K, Little P, Nakamura Y. Mathew CG, et al. Among authors: smith b. Ann Hum Genet. 1990 May;54(2):121-9. doi: 10.1111/j.1469-1809.1990.tb00368.x. Ann Hum Genet. 1990. PMID: 1974407

7

A highly polymorphic locus very tightly linked to the Huntington's disease gene.

Wasmuth JJ, Hewitt J, Smith B, Allard D, Haines JL, Skarecky D, Partlow E, Hayden MR. Wasmuth JJ, et al. Among authors: smith b. Nature. 1988 Apr 21;332(6166):734-6. doi: 10.1038/332734a0. Nature. 1988. PMID: 2895895

8

A polymorphic DNA marker that represents a conserved expressed sequence in the region of the Huntington disease gene.

Hayden MR, Hewitt J, Wasmuth JJ, Kastelein JJ, Langlois S, Conneally M, Haines J, Smith B, Hilbert C, Allard D. Hayden MR, et al. Among authors: smith b. Am J Hum Genet. 1988 Jan;42(1):125-31. Am J Hum Genet. 1988. PMID: 2892395 Free PMC article.

9

A cell hybrid and recombinant DNA library that facilitate identification of polymorphic loci in the vicinity of the Huntington disease gene.

Wasmuth JJ, Carlock LR, Smith B, Immken LL. Wasmuth JJ, et al. Among authors: smith b. Am J Hum Genet. 1986 Sep;39(3):397-403. Am J Hum Genet. 1986. PMID: 2945430 Free PMC article.

10

A new DNA marker (D4S90) is located terminally on the short arm of chromosome 4, close to the Huntington disease gene.

Youngman S, Sarfarazi M, Bucan M, MacDonald M, Smith B, Zimmer M, Gilliam C, Frischauf AM, Wasmuth JJ, Gusella JF, et al. Youngman S, et al. Among authors: smith b. Genomics. 1989 Nov;5(4):802-9. doi: 10.1016/0888-7543(89)90122-5. Genomics. 1989. PMID: 2574148

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