Volinia S - Search Results

1

A recurrent missense mutation (Arg----Gln) and a partial deletion in factor VIII gene causing severe haemophilia A.

Bernardi F, Volinia S, Patracchini P, Gemmati D, Boninsegna S, Schwienbacher C, Marchetti G. Bernardi F, et al. Among authors: volinia s. Br J Haematol. 1989 Feb;71(2):271-6. doi: 10.1111/j.1365-2141.1989.tb04266.x. Br J Haematol. 1989. PMID: 2493803

2

Characterization of the pseudogenic and genic homologous regions of von Willebrand factor.

Marchetti G, Patracchini P, Volinia S, Aiello V, Schiavoni M, Ciavarella N, Calzolari E, Schwienbacher C, Bernardi F. Marchetti G, et al. Among authors: volinia s. Br J Haematol. 1991 May;78(1):71-9. doi: 10.1111/j.1365-2141.1991.tb04385.x. Br J Haematol. 1991. PMID: 2043485

3

Direct detection of a missense mutation causing severe hemophilia A by PCR amplification and fluorescence scanning.

Marchetti G, Gemmati D, Patracchini P, Volinia S, Castagnoli A, Tosi B, Capelli M, Bernardi F. Marchetti G, et al. Among authors: volinia s. Hematol Pathol. 1990;4(4):185-8. Hematol Pathol. 1990. PMID: 2074260

4

Partial gene deletion in a family with factor X deficiency.

Bernardi F, Marchetti G, Patracchini P, Volinia S, Gemmati D, Simioni P, Girolami A. Bernardi F, et al. Among authors: volinia s. Blood. 1989 Jun;73(8):2123-7. Blood. 1989. PMID: 2567188 Free article.

5

von Willebrand disease investigated by two novel RFLPs.

Bernardi F, Guerra S, Patracchini P, Volinia S, Buzzoni D, Ballerini G, Casonato A, Marchetti G. Bernardi F, et al. Among authors: volinia s. Br J Haematol. 1988 Feb;68(2):243-8. doi: 10.1111/j.1365-2141.1988.tb06196.x. Br J Haematol. 1988. PMID: 2894837

6

A HindIII RFLP and a gene lesion in the coagulation factor VIII gene.

Bernardi F, Legnani C, Volinia S, Patracchini P, Rodorigo G, DeRosa V, Marchetti G. Bernardi F, et al. Among authors: volinia s. Hum Genet. 1988 Apr;78(4):359-62. doi: 10.1007/BF00291736. Hum Genet. 1988. PMID: 2896159

7

A frequent factor XII gene mutation in Hageman trait.

Bernardi F, Marchetti G, Volinia S, Patracchini P, Casonato A, Girolami A, Conconi F. Bernardi F, et al. Among authors: volinia s. Hum Genet. 1988 Oct;80(2):149-51. doi: 10.1007/BF00702858. Hum Genet. 1988. PMID: 3169737

8

Co-localization of rare oligonucleotides and regulatory elements in mammalian upstream gene regions.

Volinia S, Bernardi F, Gambari R, Barrai I. Volinia S, et al. J Mol Biol. 1988 Sep 20;203(2):385-90. doi: 10.1016/0022-2836(88)90006-x. J Mol Biol. 1988. PMID: 3199439

9

The frequency of oligonucleotides in mammalian genic regions.

Volinia S, Gambari R, Bernardi F, Barrai I. Volinia S, et al. Comput Appl Biosci. 1989 Feb;5(1):33-40. doi: 10.1093/bioinformatics/5.1.33. Comput Appl Biosci. 1989. PMID: 2924169

10

RFLP analysis in families with sporadic hemophilia A. Estimate of the mutation ratio in male and female gametes.

Bernardi F, Marchetti G, Bertagnolo V, Faggioli L, Volinia S, Patracchini P, Bartolai S, Vannini F, Felloni L, Rossi L, et al. Bernardi F, et al. Among authors: volinia s. Hum Genet. 1987 Jul;76(3):253-6. doi: 10.1007/BF00283618. Hum Genet. 1987. PMID: 2885255

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