Powers VE - Search Results

1

Gene on short arm of human X chromosome complements murine tsA1S9 DNA synthesis mutation.

Brown CJ, Powers VE, Munroe DL, Sheinin R, Willard HF. Brown CJ, et al. Among authors: powers ve. Somat Cell Mol Genet. 1989 Mar;15(2):173-8. doi: 10.1007/BF01535079. Somat Cell Mol Genet. 1989. PMID: 2928842

2

Physical mapping of 60 DNA markers in the p21.1----q21.3 region of the human X chromosome.

Lafrenière RG, Brown CJ, Powers VE, Carrel L, Davies KE, Barker DF, Willard HF. Lafrenière RG, et al. Among authors: powers ve. Genomics. 1991 Oct;11(2):352-63. doi: 10.1016/0888-7543(91)90143-3. Genomics. 1991. PMID: 1685139

3

Fast-twitch and slow-twitch/cardiac Ca2+ ATPase genes map to human chromosomes 16 and 12.

MacLennan DH, Brandl CJ, Champaneria S, Holland PC, Powers VE, Willard HF. MacLennan DH, et al. Among authors: powers ve. Somat Cell Mol Genet. 1987 Jul;13(4):341-6. doi: 10.1007/BF01534928. Somat Cell Mol Genet. 1987. PMID: 2842876

4

Molecular organization and haplotype analysis of centromeric DNA from human chromosome 17: implications for linkage in neurofibromatosis.

Willard HF, Greig GM, Powers VE, Waye JS. Willard HF, et al. Among authors: powers ve. Genomics. 1987 Dec;1(4):368-73. doi: 10.1016/0888-7543(87)90041-3. Genomics. 1987. PMID: 2896633

5

Molecular cytogenetics of alpha satellite DNA from chromosome 12: fluorescence in situ hybridization and description of DNA and array length polymorphisms.

Greig GM, Parikh S, George J, Powers VE, Willard HF. Greig GM, et al. Among authors: powers ve. Cytogenet Cell Genet. 1991;56(3-4):144-8. doi: 10.1159/000133071. Cytogenet Cell Genet. 1991. PMID: 1675980

6

Localization of the X inactivation centre on the human X chromosome in Xq13.

Brown CJ, Lafreniere RG, Powers VE, Sebastio G, Ballabio A, Pettigrew AL, Ledbetter DH, Levy E, Craig IW, Willard HF. Brown CJ, et al. Among authors: powers ve. Nature. 1991 Jan 3;349(6304):82-4. doi: 10.1038/349082a0. Nature. 1991. PMID: 1985270

7

Gene order on the short arm of human chromosome 11: regional assignment of the LDH A gene distal to catalase in two translocations.

Lewis WH, Goguen JM, Powers VE, Willard HF, Michalopoulos EE. Lewis WH, et al. Among authors: powers ve. Hum Genet. 1985;71(3):249-53. doi: 10.1007/BF00284584. Hum Genet. 1985. PMID: 3877676

8

Molecular analysis of gene deletion in aniridia--Wilms tumor association.

Michalopoulos EE, Bevilacqua PJ, Stokoe N, Powers VE, Willard HF, Lewis WH. Michalopoulos EE, et al. Among authors: powers ve. Hum Genet. 1985;70(2):157-62. doi: 10.1007/BF00273074. Hum Genet. 1985. PMID: 2989154

9

Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: implications for development of centromere-based genetic linkage maps.

Willard HF, Waye JS, Skolnick MH, Schwartz CE, Powers VE, England SB. Willard HF, et al. Among authors: powers ve. Proc Natl Acad Sci U S A. 1986 Aug;83(15):5611-5. doi: 10.1073/pnas.83.15.5611. Proc Natl Acad Sci U S A. 1986. PMID: 3016709 Free PMC article.

10

The beta-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus.

Glaser T, Lewis WH, Bruns GA, Watkins PC, Rogler CE, Shows TB, Powers VE, Willard HF, Goguen JM, Simola KO, et al. Glaser T, et al. Among authors: powers ve. Nature. 1986 Jun 26-Jul 2;321(6073):882-7. doi: 10.1038/321882a0. Nature. 1986. PMID: 3014343

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