Novelletto A - Search Results

1

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: novelletto a. Am J Hum Genet. 1994 Jun;54(6):959-65. Am J Hum Genet. 1994. PMID: 8198139 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

A new beta-thalassaemia frameshift mutation detected by PCR after selective hybridization to immobilized oligonucleotides.

Deidda G, Novelletto A, Hafez M, el-Ziny M, Terrenato L, Felicetti L. Deidda G, et al. Among authors: novelletto a. Br J Haematol. 1991 Sep;79(1):90-2. doi: 10.1111/j.1365-2141.1991.tb08012.x. Br J Haematol. 1991. PMID: 1911391

7

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.

8

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

9

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

10

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.

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