Persichetti F - Search Results

1

An additional HindIII polymorphism at the coagulation factor XIIIA locus.

Iodice C, Novelletto A, Malaspina P, Persichetti F. Iodice C, et al. Among authors: persichetti f. Nucleic Acids Res. 1990 Feb 11;18(3):693. doi: 10.1093/nar/18.3.693-a. Nucleic Acids Res. 1990. PMID: 1968632 Free PMC article. No abstract available.

2

The human Y chromosome shows a low level of DNA polymorphism.

Malaspina P, Persichetti F, Novelletto A, Iodice C, Terrenato L, Wolfe J, Ferraro M, Prantera G. Malaspina P, et al. Among authors: persichetti f. Ann Hum Genet. 1990 Oct;54(4):297-305. doi: 10.1111/j.1469-1809.1990.tb00385.x. Ann Hum Genet. 1990. PMID: 1980996

3

Disequilibrium of multiple DNA markers on the human Y chromosome.

Persichetti F, Blasi P, Hammer M, Malaspina P, Jodice C, Terrenato L, Novelletto A. Persichetti F, et al. Ann Hum Genet. 1992 Oct;56(4):303-10. doi: 10.1111/j.1469-1809.1992.tb01157.x. Ann Hum Genet. 1992. PMID: 1492745

4

The gene for spinal cerebellar ataxia 1 (SCA1) is flanked by two closely linked highly polymorphic microsatellite loci.

Jodice C, Frontali M, Persichetti F, Novelletto A, Pandolfo M, Spadaro M, Giunti P, Schinaia G, Lulli P, Malaspina P, et al. Jodice C, et al. Among authors: persichetti f. Hum Mol Genet. 1993 Sep;2(9):1383-7. doi: 10.1093/hmg/2.9.1383. Hum Mol Genet. 1993. PMID: 8242061

5

Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia I.

Jodice C, Malaspina P, Persichetti F, Novelletto A, Spadaro M, Giunti P, Morocutti C, Terrenato L, Harding AE, Frontali M. Jodice C, et al. Among authors: persichetti f. Am J Hum Genet. 1994 Jun;54(6):959-65. Am J Hum Genet. 1994. PMID: 8198139 Free PMC article.

6

Polymorphism analysis of the huntingtin gene in Italian families affected with Huntington disease.

Novelletto A, Persichetti F, Sabbadini G, Mandich P, Bellone E, Ajmar F, Squitieri F, Campanella G, Bozza A, MacDonald ME, et al. Novelletto A, et al. Among authors: persichetti f. Hum Mol Genet. 1994 Jul;3(7):1129-32. doi: 10.1093/hmg/3.7.1129. Hum Mol Genet. 1994. PMID: 7981682

7

Analysis of the trinucleotide repeat expansion in Italian families affected with Huntington disease.

Novelletto A, Persichetti F, Sabbadini G, Mandich P, Bellone E, Ajmar F, Pergola M, Del Senno L, MacDonald ME, Gusella JF, et al. Novelletto A, et al. Among authors: persichetti f. Hum Mol Genet. 1994 Jan;3(1):93-8. doi: 10.1093/hmg/3.1.93. Hum Mol Genet. 1994. PMID: 8162059

8

Recurrent simple tandem repeat mutations during human Y-chromosome radiation in Caucasian subpopulations.

Ciminelli BM, Pompei F, Malaspina P, Hammer M, Persichetti F, Pignatti PF, Palena A, Anagnou N, Guanti G, Jodice C, et al. Ciminelli BM, et al. Among authors: persichetti f. J Mol Evol. 1995 Dec;41(6):966-73. doi: 10.1007/BF00173177. J Mol Evol. 1995. PMID: 8587142

9

The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locus.

Kwiatkowski TJ Jr, Orr HT, Banfi S, McCall AE, Jodice C, Persichetti F, Novelletto A, LeBorgne-DeMarquoy F, Duvick LA, Frontali M, et al. Kwiatkowski TJ Jr, et al. Among authors: persichetti f. Am J Hum Genet. 1993 Aug;53(2):391-400. Am J Hum Genet. 1993. PMID: 8101039 Free PMC article.

10

Trinucleotide repeat length instability and age of onset in Huntington's disease.

Duyao M, Ambrose C, Myers R, Novelletto A, Persichetti F, Frontali M, Folstein S, Ross C, Franz M, Abbott M, et al. Duyao M, et al. Among authors: persichetti f. Nat Genet. 1993 Aug;4(4):387-92. doi: 10.1038/ng0893-387. Nat Genet. 1993. PMID: 8401587

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