Novelli G - Search Results

1

Prediction of myotonic dystrophy clinical severity based on the number of intragenic [CTG]n trinucleotide repeats.

Gennarelli M, Novelli G, Andreasi Bassi F, Martorell L, Cornet M, Menegazzo E, Mostacciuolo ML, Martinez JM, Angelini C, Pizzuti A, Baiget M, Dallapiccola B. Gennarelli M, et al. Among authors: novelli g. Am J Med Genet. 1996 Nov 11;65(4):342-7. doi: 10.1002/(SICI)1096-8628(19961111)65:4<342::AID-AJMG18>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8923947

2

The prevalence of HPV16DNA in normal and pathological cervical scrapes using the polymerase chain reaction.

Pasetto N, Sesti F, De Santis L, Piccione E, Novelli G, Dallapiccola B. Pasetto N, et al. Among authors: novelli g. Gynecol Oncol. 1992 Jul;46(1):33-6. doi: 10.1016/0090-8258(92)90191-k. Gynecol Oncol. 1992. PMID: 1321780

3

Inosine-containing primers in human papillomavirus detection by polymerase chain reaction.

Novelli G, Gennarelli M, De Santis L, Angeloni P, Dallapiccola B. Novelli G, et al. Biomed Pharmacother. 1992;46(4):167-9. doi: 10.1016/0753-3322(92)90025-3. Biomed Pharmacother. 1992. PMID: 1330051

4

Genotyping of spinal muscular atrophy families with linked DNA probes.

Gennarelli M, Melchionda S, Fattorini C, Novelli G, Dallapiccola B. Gennarelli M, et al. Among authors: novelli g. Clin Genet. 1992 Dec;42(6):317-9. doi: 10.1111/j.1399-0004.1992.tb03264.x. Clin Genet. 1992. PMID: 1362926

5

Expansion of the myotonic dystrophy gene in Italian and Spanish patients.

Melchionda S, Cobo A, Gennarelli M, Martorell L, Fattorini C, Baiget M, Lopez de Munain A, Johnson K, Shelbourne P, Novelli G, et al. Melchionda S, et al. Among authors: novelli g. J Med Genet. 1992 Nov;29(11):789-90. doi: 10.1136/jmg.29.11.789. J Med Genet. 1992. PMID: 1453428 Free PMC article.

6

Polymerase chain reaction in the detection of mRNA transcripts from the slow skeletal troponin T (TNNT1) gene in myotonic dystrophy and normal muscle.

Novelli G, Gennarelli M, Zelano G, Sangiuolo F, Lo Cicero S, Samson F, Dallapiccola B. Novelli G, et al. Cell Biochem Funct. 1992 Dec;10(4):251-6. doi: 10.1002/cbf.290100407. Cell Biochem Funct. 1992. PMID: 1473264

7

[The correlation between the genotype and the clinical expression of cystic fibrosis].

Lucidi V, Novelli G, Castro M, Sangiuolo F, Papadatou B, Ferretti F, Orrù M, Dallapiccola B. Lucidi V, et al. Among authors: novelli g. Pediatr Med Chir. 1992 Sep-Oct;14(5):513-5. Pediatr Med Chir. 1992. PMID: 1488308 Italian.

8

The cystic fibrosis delta F508 mutation in the Albanian population.

Novelli G, Sangiuolo F, Mokini V, Cikuli M, Piazza A, Dallapiccola B. Novelli G, et al. Am J Hum Genet. 1992 Apr;50(4):875-6. Am J Hum Genet. 1992. PMID: 1550133 Free PMC article. No abstract available.

9

Assignment of the slow troponin T (TNNT1) gene to chromosome 19 using polymerase chain reaction.

Novelli G, Gennarelli M, Rocchi M, Dallapiccola B. Novelli G, et al. Hum Genet. 1992 Mar;88(6):697-8. doi: 10.1007/BF02265301. Hum Genet. 1992. PMID: 1551677 No abstract available.

10

3' creatine kinase (M-type) polymorphisms linked to myotonic dystrophy in Italian and Spanish populations.

Gennarelli M, Novelli G, Cobo A, Baiget M, Dallapiccola B. Gennarelli M, et al. Among authors: novelli g. Hum Genet. 1991 Oct;87(6):654-6. doi: 10.1007/BF00201719. Hum Genet. 1991. PMID: 1682233

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