Nelson DL - Search Results

1

Molecular and phenotypic variation in patients with severe Hunter syndrome.

Timms KM, Bondeson ML, Ansari-Lari MA, Lagerstedt K, Muzny DM, Dugan-Rocha SP, Nelson DL, Pettersson U, Gibbs RA. Timms KM, et al. Among authors: nelson dl. Hum Mol Genet. 1997 Mar;6(3):479-86. doi: 10.1093/hmg/6.3.479. Hum Mol Genet. 1997. PMID: 9147653

2

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.

3

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.

4

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

5

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.

6

High resolution methylation analysis of the FMR1 gene trinucleotide repeat region in fragile X syndrome.

Hornstra IK, Nelson DL, Warren ST, Yang TP. Hornstra IK, et al. Among authors: nelson dl. Hum Mol Genet. 1993 Oct;2(10):1659-65. doi: 10.1093/hmg/2.10.1659. Hum Mol Genet. 1993. PMID: 8268919

7

Regional assignment of 19 X-linked ESTs.

Parrish JE, Nelson DL. Parrish JE, et al. Among authors: nelson dl. Hum Mol Genet. 1993 Nov;2(11):1901-5. doi: 10.1093/hmg/2.11.1901. Hum Mol Genet. 1993. PMID: 8281154

8

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. 1993 Aug;2(8):1147-53. doi: 10.1093/hmg/2.8.1147. Hum Mol Genet. 1993. PMID: 8401496

9

A muscle-specific DNase I-like gene in human Xq28.

Parrish JE, Ciccodicola A, Wehhert M, Cox GF, Chen E, Nelson DL. Parrish JE, et al. Among authors: nelson dl. Hum Mol Genet. 1995 Sep;4(9):1557-64. doi: 10.1093/hmg/4.9.1557. Hum Mol Genet. 1995. PMID: 8541839

10

An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3-Xp21.3.

Ferrero GB, Franco B, Roth EJ, Firulli BA, Borsani G, Delmas-Mata J, Weissenbach J, Halley G, Schlessinger D, Chinault AC, Zoghbi HY, Nelson DL, Ballabio A. Ferrero GB, et al. Among authors: nelson dl. Hum Mol Genet. 1995 Oct;4(10):1821-7. doi: 10.1093/hmg/4.10.1821. Hum Mol Genet. 1995. PMID: 8595402

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