Nelson DL - Search Results

1

Duplication of a gene-rich cluster between 16p11.1 and Xq28: a novel pericentromeric-directed mechanism for paralogous genome evolution.

Eichler EE, Lu F, Shen Y, Antonacci R, Jurecic V, Doggett NA, Moyzis RK, Baldini A, Gibbs RA, Nelson DL. Eichler EE, et al. Among authors: nelson dl. Hum Mol Genet. 1996 Jul;5(7):899-912. doi: 10.1093/hmg/5.7.899. Hum Mol Genet. 1996. PMID: 8817324

2

Applications of polymerase chain reaction methods in genome mapping.

Nelson DL. Nelson DL. Curr Opin Genet Dev. 1991 Jun;1(1):62-8. doi: 10.1016/0959-437x(91)80043-l. Curr Opin Genet Dev. 1991. PMID: 1688122 Review.

3

Alu-primed polymerase chain reaction for regional assignment of 110 yeast artificial chromosome clones from the human X chromosome: identification of clones associated with a disease locus.

Nelson DL, Ballabio A, Victoria MF, Pieretti M, Bies RD, Gibbs RA, Maley JA, Chinault AC, Webster TD, Caskey CT. Nelson DL, et al. Proc Natl Acad Sci U S A. 1991 Jul 15;88(14):6157-61. doi: 10.1073/pnas.88.14.6157. Proc Natl Acad Sci U S A. 1991. PMID: 2068096 Free PMC article.

4

A de novo deletion in FMR1 in a patient with developmental delay.

Gu Y, Lugenbeel KA, Vockley JG, Grody WW, Nelson DL. Gu Y, et al. Among authors: nelson dl. Hum Mol Genet. 1994 Sep;3(9):1705-6. doi: 10.1093/hmg/3.9.1705. Hum Mol Genet. 1994. PMID: 7530551 No abstract available.

5

Evolution of the cryptic FMR1 CGG repeat.

Eichler EE, Kunst CB, Lugenbeel KA, Ryder OA, Davison D, Warren ST, Nelson DL. Eichler EE, et al. Among authors: nelson dl. Nat Genet. 1995 Nov;11(3):301-8. doi: 10.1038/ng1195-301. Nat Genet. 1995. PMID: 7581454

6

Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomes.

van den Ouweland AM, Deelen WH, Kunst CB, Uzielli ML, Nelson DL, Warren ST, Oostra BA, Halley DJ. van den Ouweland AM, et al. Among authors: nelson dl. Hum Mol Genet. 1994 Oct;3(10):1823-7. doi: 10.1093/hmg/3.10.1823. Hum Mol Genet. 1994. PMID: 7849707

7

Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE.

Parrish JE, Oostra BA, Verkerk AJ, Richards CS, Reynolds J, Spikes AS, Shaffer LG, Nelson DL. Parrish JE, et al. Among authors: nelson dl. Nat Genet. 1994 Nov;8(3):229-35. doi: 10.1038/ng1194-229. Nat Genet. 1994. PMID: 7874164

8

Robust amplification and ethidium-visible detection of the fragile X syndrome CGG repeat using Pfu polymerase.

Chong SS, Eichler EE, Nelson DL, Hughes MR. Chong SS, et al. Among authors: nelson dl. Am J Med Genet. 1994 Jul 15;51(4):522-6. doi: 10.1002/ajmg.1320510447. Am J Med Genet. 1994. PMID: 7943034

9

Length of uninterrupted CGG repeats determines instability in the FMR1 gene.

Eichler EE, Holden JJ, Popovich BW, Reiss AL, Snow K, Thibodeau SN, Richards CS, Ward PA, Nelson DL. Eichler EE, et al. Among authors: nelson dl. Nat Genet. 1994 Sep;8(1):88-94. doi: 10.1038/ng0994-88. Nat Genet. 1994. PMID: 7987398

10

Fine structure of the human FMR1 gene.

Eichler EE, Richards S, Gibbs RA, Nelson DL. Eichler EE, et al. Among authors: nelson dl. Hum Mol Genet. 1994 Apr;3(4):684-5. Hum Mol Genet. 1994. PMID: 8069329 No abstract available.

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