Ward PA - 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: ward pa. Nat Genet. 1994 Sep;8(1):88-94. doi: 10.1038/ng0994-88. Nat Genet. 1994. PMID: 7987398

2

Population survey of the human FMR1 CGG repeat substructure suggests biased polarity for the loss of AGG interruptions.

Eichler EE, Hammond HA, Macpherson JN, Ward PA, Nelson DL. Eichler EE, et al. Among authors: ward pa. Hum Mol Genet. 1995 Dec;4(12):2199-208. doi: 10.1093/hmg/4.12.2199. Hum Mol Genet. 1995. PMID: 8634688

3

Effects of the sex of myotonic dystrophy patients on the unstable triplet repeat in their affected offspring.

Ashizawa T, Dunne PW, Ward PA, Seltzer WK, Richards CS. Ashizawa T, et al. Among authors: ward pa. Neurology. 1994 Jan;44(1):120-2. doi: 10.1212/wnl.44.1.120. Neurology. 1994. PMID: 8290046

4

Screening for 185delAG in the Ashkenazim.

Richards CS, Ward PA, Roa BB, Friedman LC, Boyd AA, Kuenzli G, Dunn JK, Plon SE. Richards CS, et al. Among authors: ward pa. Am J Hum Genet. 1997 May;60(5):1085-98. Am J Hum Genet. 1997. PMID: 9150156 Free PMC article.

5

Prenatal diagnosis of Duchenne muscular dystrophy: prospective linkage analysis and retrospective dystrophin cDNA analysis.

Ward PA, Hejtmancik JF, Witkowski JA, Baumbach LL, Gunnell S, Speer J, Hawley P, Tantravahi U, Caskey CT. Ward PA, et al. Am J Hum Genet. 1989 Feb;44(2):270-81. Am J Hum Genet. 1989. PMID: 2643315 Free PMC article.

6

Premature chain termination mutation causing Duchenne muscular dystrophy.

Clemens PR, Ward PA, Caskey CT, Bulman DE, Fenwick RG. Clemens PR, et al. Among authors: ward pa. Neurology. 1992 Sep;42(9):1775-82. doi: 10.1212/wnl.42.9.1775. Neurology. 1992. PMID: 1513469

7

Congenital 21-hydroxylase deficiency as a new deletion mutation. Detection in a proband during subsequent prenatal diagnosis by HLA typing and DNA analysis.

Hejtmancik JF, Black S, Harris S, Ward PA, Callaway C, Ledbetter D, Morris J, Leech SH, Pollack MS. Hejtmancik JF, et al. Among authors: ward pa. Hum Immunol. 1992 Dec;35(4):246-52. doi: 10.1016/0198-8859(92)90006-9. Hum Immunol. 1992. PMID: 1293088

8

DMD carrier detection and prenatal diagnosis via recombinant DNA methods.

Caskey CT, Ward P, Hejtmancik F. Caskey CT, et al. Adv Neurol. 1988;48:83-91. Adv Neurol. 1988. PMID: 2891260 No abstract available.

9

Direct molecular genetic diagnosis and heterozygote identification in X-linked Emery-Dreifuss muscular dystrophy by heteroduplex analysis.

Wulff K, Ebener U, Wehnert CS, Ward PA, Reuner U, Hiebsch W, Herrmann FH, Wehnert M. Wulff K, et al. Among authors: ward pa. Dis Markers. 1997 Apr;13(2):77-86. Dis Markers. 1997. PMID: 9160182

10

Molecular and clinical correlations of deletions leading to Duchenne and Becker muscular dystrophies.

Baumbach LL, Chamberlain JS, Ward PA, Farwell NJ, Caskey CT. Baumbach LL, et al. Among authors: ward pa. Neurology. 1989 Apr;39(4):465-74. doi: 10.1212/wnl.39.4.465. Neurology. 1989. PMID: 2927671

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