Papp AC - Search Results

1

Exon 44 nonsense mutation in two-Duchenne muscular dystrophy brothers detected by heteroduplex analysis.

Prior TW, Papp AC, Snyder PJ, Burghes AH, Sedra MS, Western LM, Bartolo C, Mendell JR. Prior TW, et al. Among authors: papp ac. Hum Mutat. 1993;2(3):192-5. doi: 10.1002/humu.1380020307. Hum Mutat. 1993. PMID: 8364587

2

Characterization of translational frame exception patients in Duchenne/Becker muscular dystrophy.

Winnard AV, Klein CJ, Coovert DD, Prior T, Papp A, Snyder P, Bulman DE, Ray PN, McAndrew P, King W, et al. Winnard AV, et al. Hum Mol Genet. 1993 Jun;2(6):737-44. doi: 10.1093/hmg/2.6.737. Hum Mol Genet. 1993. PMID: 8353493

3

Case of the month: germline mosaicism in carriers of Duchenne muscular dystrophy.

Prior TW, Papp AC, Snyder PJ, Mendell JR. Prior TW, et al. Among authors: papp ac. Muscle Nerve. 1992 Aug;15(8):960-3. doi: 10.1002/mus.880150815. Muscle Nerve. 1992. PMID: 1353862

4

A HindIII/BglII dystrophin gene polymorphism in the African-American population.

Prior TW, Papp AC, Snyder PJ, Burghes AH, Wallace BH. Prior TW, et al. Among authors: papp ac. Hum Genet. 1992 Aug;89(6):687-8. doi: 10.1007/BF00221965. Hum Genet. 1992. PMID: 1355070

5

Optimization of DNA extraction from formalin-fixed tissue and its clinical application in Duchenne muscular dystrophy.

Forsthoefel KF, Papp AC, Snyder PJ, Prior TW. Forsthoefel KF, et al. Among authors: papp ac. Am J Clin Pathol. 1992 Jul;98(1):98-104. doi: 10.1093/ajcp/98.1.98. Am J Clin Pathol. 1992. PMID: 1615933

6

Determination of carrier status in Duchenne and Becker muscular dystrophies by quantitative polymerase chain reaction and allele-specific oligonucleotides.

Prior TW, Papp AC, Snyder PJ, Highsmith WE Jr, Friedman KJ, Perry TR, Silverman LM, Mendell JR. Prior TW, et al. Among authors: papp ac. Clin Chem. 1990 Dec;36(12):2113-7. Clin Chem. 1990. PMID: 2253356

7

Rapid DNA haplotyping using a multiplex heteroduplex approach: application to Duchenne muscular dystrophy carrier testing.

Prior TW, Wenger GD, Papp AC, Snyder PJ, Sedra MS, Bartolo C, Moore JW, Highsmith WE. Prior TW, et al. Among authors: papp ac. Hum Mutat. 1995;5(3):263-8. doi: 10.1002/humu.1380050312. Hum Mutat. 1995. PMID: 7599638

8

Spectrum of small mutations in the dystrophin coding region.

Prior TW, Bartolo C, Pearl DK, Papp AC, Snyder PJ, Sedra MS, Burghes AH, Mendell JR. Prior TW, et al. Among authors: papp ac. Am J Hum Genet. 1995 Jul;57(1):22-33. Am J Hum Genet. 1995. PMID: 7611292 Free PMC article.

9

Identification of a missense mutation, single base deletion and a polymorphism in the dystrophin exon 16.

Prior TW, Bartolo C, Papp AC, Snyder PJ, Sedra MS, Burghes AH, Mendell JR. Prior TW, et al. Among authors: papp ac. Hum Mol Genet. 1994 Jul;3(7):1173-4. doi: 10.1093/hmg/3.7.1173. Hum Mol Genet. 1994. PMID: 7981690 No abstract available.

10

Detection of an exon 53 polymorphism in the dystrophin gene.

Prior TW, Papp AC, Snyder PJ, Sedra MS. Prior TW, et al. Among authors: papp ac. Hum Genet. 1993 Oct 1;92(3):302-4. doi: 10.1007/BF00244477. Hum Genet. 1993. PMID: 8104863

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