Novelletto A - Search Results

1

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: novelletto a. Hum Mol Genet. 1993 Sep;2(9):1383-7. doi: 10.1093/hmg/2.9.1383. Hum Mol Genet. 1993. PMID: 8242061

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

Molecular characterization of beta-thalassemia mutations in Egypt.

Novelletto A, Hafez M, Deidda G, Di Rienzo A, Felicetti L, el-Tahan H, el Morsi Z, el-Ziny M, al-Tonbary Y, Sittien A, et al. Novelletto A, et al. Hum Genet. 1990 Aug;85(3):272-4. doi: 10.1007/BF00206744. Hum Genet. 1990. PMID: 1975554

8

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

9

Protection against malaria morbidity: near-fixation of the alpha-thalassemia gene in a Nepalese population.

Modiano G, Morpurgo G, Terrenato L, Novelletto A, Di Rienzo A, Colombo B, Purpura M, Mariani M, Santachiara-Benerecetti S, Brega A, et al. Modiano G, et al. Among authors: novelletto a. Am J Hum Genet. 1991 Feb;48(2):390-7. Am J Hum Genet. 1991. PMID: 1990845 Free PMC article.

10

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

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