Ferrari M - Search Results

1

Molecular characterization of Italian chromosomes carrying the Lepore Boston gene.

Camaschella C, Serra A, Bertero MT, Gottardi E, Alfarano A, Revello D, Travi M, Seia M, Cremonesi L, Ferrari M. Camaschella C, et al. Among authors: ferrari m. Acta Haematol. 1989;81(3):136-9. doi: 10.1159/000205545. Acta Haematol. 1989. PMID: 2565641

2

Meiotic recombination in the beta globin gene cluster causing an error in prenatal diagnosis of beta thalassaemia.

Camaschella C, Serra A, Saglio G, Bertero MT, Mazza U, Terzoli S, Brambati B, Cremonesi L, Travi M, Ferrari M. Camaschella C, et al. Among authors: ferrari m. J Med Genet. 1988 May;25(5):307-10. doi: 10.1136/jmg.25.5.307. J Med Genet. 1988. PMID: 2898535 Free PMC article.

3

Molecular characterization of hemoglobin C in Sicily.

Travi M, Cremonesi L, Primignani P, Di Benedetto S, Testa R, Schilirò G, Ferrari M. Travi M, et al. Among authors: ferrari m. Am J Hematol. 1992 Jan;39(1):5-8. doi: 10.1002/ajh.2830390103. Am J Hematol. 1992. PMID: 1346948

4

First trimester diagnosis of beta-thalassemia by DNA polymorphism analysis in the Italian population.

Ferrari M, Cremonesi L, Travi M, Seia M, Cantù-Rajnoldi A, Sampietro M, Brambati B, Gabutti W, Campogrande M, Saglio G, et al. Ferrari M, et al. Birth Defects Orig Artic Ser. 1988;23(5B):465-70. Birth Defects Orig Artic Ser. 1988. PMID: 3390575 No abstract available.

5

Evidence for the single origin of HB G-San Jose in Sicily.

Cremonesi L, Travi M, Li Volti S, Testa R, Schiliro G, Ferrari M. Cremonesi L, et al. Among authors: ferrari m. Hemoglobin. 1989;13(6):579-84. doi: 10.3109/03630268908993108. Hemoglobin. 1989. PMID: 2575088

6

Fetal diagnosis of beta-thalassaemia by DNA analysis in Italy.

Camaschella C, Saglio G, Serra A, Cremonesi L, Travi M, Ferrari M. Camaschella C, et al. Among authors: ferrari m. Lancet. 1986 Feb 15;1(8477):390. doi: 10.1016/s0140-6736(86)92359-7. Lancet. 1986. PMID: 2868332 No abstract available.

7

Search for mutations in pancreatic sufficient cystic fibrosis Italian patients: detection of 90% of molecular defects and identification of three novel mutations.

Brancolini V, Cremonesi L, Belloni E, Pappalardo E, Bordoni R, Seia M, Russo S, Padoan R, Giunta A, Ferrari M. Brancolini V, et al. Among authors: ferrari m. Hum Genet. 1995 Sep;96(3):312-8. doi: 10.1007/BF00210414. Hum Genet. 1995. PMID: 7544319

8

A TaqI RFLP of the human plasminogen gene.

Candiani G, Cremonesi L, Bruno L, Tenan M, Ferrari M, Camerino G, Taramelli R. Candiani G, et al. Among authors: ferrari m. Nucleic Acids Res. 1989 Nov 11;17(21):8900. doi: 10.1093/nar/17.21.8900. Nucleic Acids Res. 1989. PMID: 2573885 Free PMC article. No abstract available.

9

Screening for non-delta F508 mutations in five exons of the cystic fibrosis transmembrane conductance regulator (CFTR) gene in Italy.

Devoto M, Ronchetto P, Fanen P, Orriols JJ, Romeo G, Goossens M, Ferrari M, Magnani C, Seia M, Cremonesi L. Devoto M, et al. Among authors: ferrari m. Am J Hum Genet. 1991 Jun;48(6):1127-32. Am J Hum Genet. 1991. PMID: 1709778 Free PMC article.

10

Informativity of intragenic microsatellites for carrier detection and prenatal diagnosis of cystic fibrosis in the Italian population.

Magnani C, Cremonesi L, Belloni E, Ferrari M, Seia M, Russo MP, Devoto M, Ronchetto P, Romeo G. Magnani C, et al. Among authors: ferrari m. Clin Genet. 1994 Mar;45(3):135-9. doi: 10.1111/j.1399-0004.1994.tb04010.x. Clin Genet. 1994. PMID: 7913006

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