Nelson DL - Search Results

1

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

2

The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphatase.

Attree O, Olivos IM, Okabe I, Bailey LC, Nelson DL, Lewis RA, McInnes RR, Nussbaum RL. Attree O, et al. Among authors: nelson dl. Nature. 1992 Jul 16;358(6383):239-42. doi: 10.1038/358239a0. Nature. 1992. PMID: 1321346

3

Triplet repeat mutations in human disease.

Caskey CT, Pizzuti A, Fu YH, Fenwick RG Jr, Nelson DL. Caskey CT, et al. Among authors: nelson dl. Science. 1992 May 8;256(5058):784-9. doi: 10.1126/science.1589758. Science. 1992. PMID: 1589758 Review.

4

Intragenic probe used for diagnostics in fragile X families.

Verkerk AJ, deVries BB, Niermeijer MF, Fu YH, Nelson DL, Warren ST, Majoor-Krakauer DF, Halley DJ, Oostra BA. Verkerk AJ, et al. Among authors: nelson dl. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):192-6. doi: 10.1002/ajmg.1320430132. Am J Med Genet. 1992. PMID: 1605192

5

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.

6

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.

7

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

8

The fragile X syndromes.

Nelson DL. Nelson DL. Semin Cell Biol. 1995 Feb;6(1):5-11. doi: 10.1016/1043-4682(95)90009-8. Semin Cell Biol. 1995. PMID: 7620122 Review.

9

Intragenic loss of function mutations demonstrate the primary role of FMR1 in fragile X syndrome.

Lugenbeel KA, Peier AM, Carson NL, Chudley AE, Nelson DL. Lugenbeel KA, et al. Among authors: nelson dl. Nat Genet. 1995 Aug;10(4):483-5. doi: 10.1038/ng0895-483. Nat Genet. 1995. PMID: 7670500

10

The fragile X premutation in carriers and its effect on mutation size in offspring.

Fisch GS, Snow K, Thibodeau SN, Chalifaux M, Holden JJ, Nelson DL, Howard-Peebles PN, Maddalena A. Fisch GS, et al. Among authors: nelson dl. Am J Hum Genet. 1995 May;56(5):1147-55. Am J Hum Genet. 1995. PMID: 7726171 Free PMC article.

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