Popovich B - Search Results

1

Fluorescent multiplex linkage analysis and carrier detection for Duchenne/Becker muscular dystrophy.

Schwartz LS, Tarleton J, Popovich B, Seltzer WK, Hoffman EP. Schwartz LS, et al. Among authors: popovich b. Am J Hum Genet. 1992 Oct;51(4):721-9. Am J Hum Genet. 1992. PMID: 1415217 Free PMC article.

2

Uniparental disomy of the entire X chromosome in a female with Duchenne muscular dystrophy.

Quan F, Janas J, Toth-Fejel S, Johnson DB, Wolford JK, Popovich BW. Quan F, et al. Among authors: popovich bw. Am J Hum Genet. 1997 Jan;60(1):160-5. Am J Hum Genet. 1997. PMID: 8981959 Free PMC article.

3

The impact of imprinting: Prader-Willi syndrome resulting from chromosome translocation, recombination, and nondisjunction.

Toth-Fejel S, Olson S, Gunter K, Quan F, Wolford J, Popovich BW, Magenis RE. Toth-Fejel S, et al. Among authors: popovich bw. Am J Hum Genet. 1996 May;58(5):1008-16. Am J Hum Genet. 1996. PMID: 8651261 Free PMC article.

4

Hypomethylation of an expanded FMR1 allele is not associated with a global DNA methylation defect.

Burman RW, Yates PA, Green LD, Jacky PB, Turker MS, Popovich BW. Burman RW, et al. Among authors: popovich bw. Am J Hum Genet. 1999 Nov;65(5):1375-86. doi: 10.1086/302628. Am J Hum Genet. 1999. PMID: 10521303 Free PMC article.

5

Fully expanded FMR1 CGG repeats exhibit a length- and differentiation-dependent instability in cell hybrids that is independent of DNA methylation.

Burman RW, Popovich BW, Jacky PB, Turker MS. Burman RW, et al. Among authors: popovich bw. Hum Mol Genet. 1999 Nov;8(12):2293-302. doi: 10.1093/hmg/8.12.2293. Hum Mol Genet. 1999. PMID: 10545610

6

A novel CAG repeat configuration in the SCA1 gene: implications for the molecular diagnostics of spinocerebellar ataxia type 1.

Quan F, Janas J, Popovich BW. Quan F, et al. Among authors: popovich bw. Hum Mol Genet. 1995 Dec;4(12):2411-3. doi: 10.1093/hmg/4.12.2411. Hum Mol Genet. 1995. PMID: 8634720 No abstract available.

7

Technical standards and guidelines for fragile X: the first of a series of disease-specific supplements to the Standards and Guidelines for Clinical Genetics Laboratories of the American College of Medical Genetics. Quality Assurance Subcommittee of the Laboratory Practice Committee.

Maddalena A, Richards CS, McGinniss MJ, Brothman A, Desnick RJ, Grier RE, Hirsch B, Jacky P, McDowell GA, Popovich B, Watson M, Wolff DJ. Maddalena A, et al. Among authors: popovich b. Genet Med. 2001 May-Jun;3(3):200-5. doi: 10.1097/00125817-200105000-00010. Genet Med. 2001. PMID: 11388762 Free PMC article.

8

An atypical case of fragile X syndrome caused by a deletion that includes the FMR1 gene.

Quan F, Zonana J, Gunter K, Peterson KL, Magenis RE, Popovich BW. Quan F, et al. Among authors: popovich bw. Am J Hum Genet. 1995 May;56(5):1042-51. Am J Hum Genet. 1995. PMID: 7726157 Free PMC article.

9

Fragile X full mutations are more similar in siblings than in unrelated patients: further evidence for a familial factor in CGG repeat dynamics.

Burman RW, Anoe KS, Popovich BW. Burman RW, et al. Among authors: popovich bw. Genet Med. 2000 Jul-Aug;2(4):242-8. doi: 10.1097/00125817-200007000-00007. Genet Med. 2000. PMID: 11252709 Free article.

10

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: popovich bw. Nat Genet. 1994 Sep;8(1):88-94. doi: 10.1038/ng0994-88. Nat Genet. 1994. PMID: 7987398

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