Sangiuolo F - Search Results

1

Polymorphic DNA haplotypes and delta F508 deletion in 212 Italian CF families.

Novelli G, Gasparini P, Savoia A, Pignatti PF, Sangiuolo F, Dallapiccola B. Novelli G, et al. Among authors: sangiuolo f. Hum Genet. 1990 Sep;85(4):420-1. doi: 10.1007/BF02428291. Hum Genet. 1990. PMID: 2210757

2

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. Among authors: sangiuolo f. Cell Biochem Funct. 1992 Dec;10(4):251-6. doi: 10.1002/cbf.290100407. Cell Biochem Funct. 1992. PMID: 1473264

3

[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: sangiuolo f. Pediatr Med Chir. 1992 Sep-Oct;14(5):513-5. Pediatr Med Chir. 1992. PMID: 1488308 Italian.

4

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. Among authors: sangiuolo f. Am J Hum Genet. 1992 Apr;50(4):875-6. Am J Hum Genet. 1992. PMID: 1550133 Free PMC article. No abstract available.

5

A serine-to-arginine (AGT-to-CGT) mutation in codon 549 of the CFTR gene in an Italian patient with severe cystic fibrosis.

Sangiuolo F, Novelli G, Murru S, Dallapiccola B. Sangiuolo F, et al. Genomics. 1991 Apr;9(4):788-9. doi: 10.1016/0888-7543(91)90380-w. Genomics. 1991. PMID: 1903761 No abstract available.

6

Analysis of 14 cystic fibrosis mutations in five south European populations.

Nunes V, Gasparini P, Novelli G, Gaona A, Bonizzato A, Sangiuolo F, Balassopoulou A, Giménez FJ, Dognini M, Ravnik-Glavac M, et al. Nunes V, et al. Among authors: sangiuolo f. Hum Genet. 1991 Oct;87(6):737-8. doi: 10.1007/BF00201737. Hum Genet. 1991. PMID: 1937479

7

Forensic applications of molecular genetic analysis: an Italian collaborative study on paternity testing by the determination of variable number of tandem repeat DNA polymorphisms.

Gasparini P, Mandich P, Novelli G, Bellone E, Sangiuolo F, De Stefano F, Potenza L, Trabetti E, Marigo M, Pignatti PF, et al. Gasparini P, et al. Among authors: sangiuolo f. Hum Hered. 1991;41(3):174-81. doi: 10.1159/000153997. Hum Hered. 1991. PMID: 1937491

8

The search for south European cystic fibrosis mutations: identification of two new mutations, four variants, and intronic sequences.

Gasparini P, Nunes V, Savoia A, Dognini M, Morral N, Gaona A, Bonizzato A, Chillon M, Sangiuolo F, Novelli G, et al. Gasparini P, et al. Among authors: sangiuolo f. Genomics. 1991 May;10(1):193-200. doi: 10.1016/0888-7543(91)90500-e. Genomics. 1991. PMID: 2045102

9

Delta F508 gene deletion and prenatal diagnosis of cystic fibrosis in Italian and Spanish families.

Novelli G, Sangiuolo F, Dallapiccola B, Gasparini P, Savoia A, Pignatti PF, Fernandez E, Benitez J, Casals T, Nunes V, et al. Novelli G, et al. Among authors: sangiuolo f. Prenat Diagn. 1990 Jun;10(6):413-4. doi: 10.1002/pd.1970100609. Prenat Diagn. 1990. PMID: 2217081 No abstract available.

10

Molecular characterization of a frameshift mutation in exon 19 of the CFTR gene.

Sangiuolo F, Lo Cicero S, Maceratesi P, Quattrucci S, Novelli G, Dallapiccola B. Sangiuolo F, et al. Hum Mutat. 1993;2(5):422-4. doi: 10.1002/humu.1380020517. Hum Mutat. 1993. PMID: 7504970 No abstract available.

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