Jodice C - 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. Am J Hum Genet. 1994 Jun;54(6):959-65. Am J Hum Genet. 1994. PMID: 8198139 Free PMC article.

2

Autosomal dominant pure cerebellar ataxia. Neurological and genetic study.

Frontali M, Spadaro M, Giunti P, Bianco F, Jodice C, Persichetti F, Colazza GB, Lulli P, Terrenato L, Morocutti C. Frontali M, et al. Among authors: jodice c. Brain. 1992 Dec;115 ( Pt 6):1647-54. doi: 10.1093/brain/115.6.1647. Brain. 1992. PMID: 1486455

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: jodice c. 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

HLA-linked spinocerebellar ataxia: a clinical and genetic study of large Italian kindreds.

Spadaro M, Giunti P, Lulli P, Frontali M, Jodice C, Cappellacci S, Morellini M, Persichetti F, Trabace S, Anastasi R, et al. Spadaro M, et al. Among authors: jodice c. Acta Neurol Scand. 1992 Apr;85(4):257-65. doi: 10.1111/j.1600-0404.1992.tb04041.x. Acta Neurol Scand. 1992. PMID: 1585797

5

The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindreds.

Zoghbi HY, Jodice C, Sandkuijl LA, Kwiatkowski TJ Jr, McCall AE, Huntoon SA, Lulli P, Spadaro M, Litt M, Cann HM, et al. Zoghbi HY, et al. Among authors: jodice c. Am J Hum Genet. 1991 Jul;49(1):23-30. Am J Hum Genet. 1991. PMID: 2063871 Free PMC article.

6

The EUROGEM map of human chromosome 6.

Terrenato L, Jodice C, Blasi P, Loizedda A, Contu L, Buard J, Vergnaud G, Humphries P, Kumar-Singh R, Massart C, et al. Terrenato L, et al. Among authors: jodice c. Eur J Hum Genet. 1994;2(3):214-5. Eur J Hum Genet. 1994. PMID: 7834286 No abstract available.

7

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: jodice c. Brain. 1994 Aug;117 ( Pt 4):645-9. doi: 10.1093/brain/117.4.645. Brain. 1994. PMID: 7922453 Free article.

8

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

9

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

10

Allele and haplotype frequency distribution of the EcoRI, RsaI, and MspI COL1A2 RFLPs among various human populations.

Pepe G, Rickards O, Jodice C, Modiano G. Pepe G, et al. Among authors: jodice c. Hum Biol. 1995 Dec;67(6):905-20. Hum Biol. 1995. PMID: 8543299

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