Pericak-Vance MA - Search Results

1

Genetic complexity and Parkinson's disease. Deane Laboratory Parkinson Disease Research Group.

Scott WK, Staijich JM, Yamaoka LH, Speer MC, Vance JM, Roses AD, Pericak-Vance MA. Scott WK, et al. Science. 1997 Jul 18;277(5324):387-8; author reply 389. doi: 10.1126/science.277.5324.387. Science. 1997. PMID: 9518366 No abstract available.

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

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. J Clin Endocrinol Metab. 1992 Jul;75(1):201-6. doi: 10.1210/jcem.75.1.1352307. J Clin Endocrinol Metab. 1992. PMID: 1352307

6

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

7

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

8

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

9

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

10

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.

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