Novelletto A - Search Results

1

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: novelletto a. Am J Hum Genet. 1993 Aug;53(2):391-400. Am J Hum Genet. 1993. PMID: 8101039 Free PMC article.

2

DNA markers in diagnosis of adult dominant polycystic kidney disease.

Veneziano L, D'Angelo AR, Burrai L, Perugia G, Gentile V, Potenza L, Iampieri MP, Novelletto A, Novelli G, Frontali M. Veneziano L, et al. Among authors: novelletto a. Eur Urol. 1992;21 Suppl 1:57-9. doi: 10.1159/000474892. Eur Urol. 1992. PMID: 1425839

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. Among authors: novelletto a. 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

Spinocerebellar ataxia (SCA1) in two large Italian kindreds: evidence in favour of a locus position distal to GLO1 and the HLA cluster.

Frontali M, Iodice C, Lulli P, Spadaro M, Cappellacci S, Giunti P, Malaspina P, Morellini M, Morocutti C, Novelletto A. Frontali M, et al. Among authors: novelletto a. Ann Hum Genet. 1991 Jan;55(1):7-15. doi: 10.1111/j.1469-1809.1991.tb00393.x. Ann Hum Genet. 1991. PMID: 1675045

5

Non-random association between DNA markers and Huntington disease locus in the Italian population.

Novelletto A, Mandich P, Bellone E, Malaspina P, Vivona G, Ajmar F, Frontali M. Novelletto A, et al. Am J Med Genet. 1991 Sep 1;40(3):374-6. doi: 10.1002/ajmg.1320400326. Am J Med Genet. 1991. PMID: 1683157

6

An additional HindIII polymorphism at the coagulation factor XIIIA locus.

Iodice C, Novelletto A, Malaspina P, Persichetti F. Iodice C, et al. Among authors: novelletto a. 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.

7

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: novelletto a. Ann Hum Genet. 1990 Oct;54(4):297-305. doi: 10.1111/j.1469-1809.1990.tb00385.x. Ann Hum Genet. 1990. PMID: 1980996

8

Epidemiological and linkage studies on Huntington's disease in Italy.

Frontali M, Malaspina P, Rossi C, Jacopini AG, Vivona G, Pergola MS, Palena A, Novelletto A. Frontali M, et al. Among authors: novelletto a. Hum Genet. 1990 Jul;85(2):165-70. doi: 10.1007/BF00193190. Hum Genet. 1990. PMID: 2142473

9

The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias.

Giunti P, Sweeney MG, Spadaro M, Jodice C, Novelletto A, Malaspina P, Frontali M, Harding AE. Giunti P, et al. Among authors: novelletto a. Brain. 1994 Aug;117 ( Pt 4):645-9. doi: 10.1093/brain/117.4.645. Brain. 1994. PMID: 7922453 Free article.

10

Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral muscular dystrophy (FSHD).

Cacurri S, Deidda G, Piazzo N, Novelletto A, La Cesa I, Servidei S, Galluzzi G, Wijmenga C, Frants RR, Felicetti L. Cacurri S, et al. Among authors: novelletto a. Hum Genet. 1994 Oct;94(4):367-74. doi: 10.1007/BF00201595. Hum Genet. 1994. PMID: 7927331

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