Pericak-Vance MA - Search Results

1

Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q.

Ben Othmane K, Hentati F, Lennon F, Ben Hamida C, Blel S, Roses AD, Pericak-Vance MA, Ben Hamida M, Vance JM. Ben Othmane K, et al. Hum Mol Genet. 1993 Oct;2(10):1625-8. doi: 10.1093/hmg/2.10.1625. Hum Mol Genet. 1993. PMID: 8268915

2

Genetic linkage studies in Huntington disease.

Pericak-Vance MA, Conneally PM, Merritt AD, Roos R, Norton JA Jr, Vance JM. Pericak-Vance MA, et al. Cytogenet Cell Genet. 1978;22(1-6):640-5. doi: 10.1159/000131042. Cytogenet Cell Genet. 1978. PMID: 156628 No abstract available.

3

Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q.

Ben Othmane K, Ben Hamida M, Pericak-Vance MA, Ben Hamida C, Blel S, Carter SC, Bowcock AM, Petruhkin K, Gilliam TC, Roses AD, et al. Ben Othmane K, et al. Nat Genet. 1992 Dec;2(4):315-7. doi: 10.1038/ng1292-315. Nat Genet. 1992. PMID: 1303286

4

Recombination of 4p16 DNA markers in an unusual family with Huntington disease.

Pritchard C, Zhu N, Zuo J, Bull L, Pericak-Vance MA, Vance JM, Roses AD, Milatovich A, Francke U, Cox DR, et al. Pritchard C, et al. Am J Hum Genet. 1992 Jun;50(6):1218-30. Am J Hum Genet. 1992. PMID: 1350884 Free PMC article.

5

Linkage studies in Charcot-Marie-Tooth disease type 2: evidence that CMT types 1 and 2 are distinct genetic entities.

Loprest LJ, Pericak-Vance MA, Stajich J, Gaskell PC, Lucas AM, Lennon F, Yamaoka LH, Roses AD, Vance JM. Loprest LJ, et al. Neurology. 1992 Mar;42(3 Pt 1):597-601. doi: 10.1212/wnl.42.3.597. Neurology. 1992. PMID: 1549221

6

North Carolina macular dystrophy is assigned to chromosome 6.

Small KW, Weber JL, Roses A, Lennon F, Vance JM, Pericak-Vance MA. Small KW, et al. Genomics. 1992 Jul;13(3):681-5. doi: 10.1016/0888-7543(92)90141-e. Genomics. 1992. PMID: 1639395

7

Support of linkage of Gerstmann-Sträussler-Scheinker syndrome to the prion protein gene on chromosome 20p12-pter.

Speer MC, Goldgaber D, Goldfarb LG, Roses AD, Pericak-Vance MA. Speer MC, et al. Genomics. 1991 Feb;9(2):366-8. doi: 10.1016/0888-7543(91)90266-h. Genomics. 1991. PMID: 1672296

8

Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2.

Vance JM, Barker D, Yamaoka LH, Stajich JM, Loprest L, Hung WY, Fischbeck K, Roses AD, Pericak-Vance MA. Vance JM, et al. Genomics. 1991 Apr;9(4):623-8. doi: 10.1016/0888-7543(91)90355-i. Genomics. 1991. PMID: 1674726

9

RsaI RFLP for electron transport flavoprotein-beta(ETFB).

Royal V, Alberts MJ, Pericak-Vance MA, Finocchiaro G, Bebout J, Yamaoka L, Hung WY, Gaskell PC, Roses AD. Royal V, et al. Nucleic Acids Res. 1991 Jul 25;19(14):4021. doi: 10.1093/nar/19.14.4021. Nucleic Acids Res. 1991. PMID: 1677763 Free PMC article.

10

Genetic linkage analysis of nerve growth factor (beta) in familial Alzheimer's disease.

Alberts MJ, Pericak-Vance MA, Royal V, Bebout J, Gaskell P, Thomas J, Hung WY, Clark C, Earl N, Roses AD. Alberts MJ, et al. Ann Neurol. 1991 Aug;30(2):216-9. doi: 10.1002/ana.410300217. Ann Neurol. 1991. PMID: 1680304

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