Bernardi F - Search Results

1

C6orf10 Low-Frequency and Rare Variants in Italian Multiple Sclerosis Patients.

Ziliotto N, Marchetti G, Scapoli C, Bovolenta M, Meneghetti S, Benazzo A, Lunghi B, Balestra D, Laino LA, Bozzini N, Guidi I, Salvi F, Straudi S, Gemmati D, Menegatti E, Zamboni P, Bernardi F. Ziliotto N, et al. Among authors: bernardi f. Front Genet. 2019 Jun 26;10:573. doi: 10.3389/fgene.2019.00573. eCollection 2019. Front Genet. 2019. PMID: 31297130 Free PMC article.

2

Characterization and mapping of the 5' portion of von Willebrand factor pseudogene.

Patracchini P, Marchetti G, Aiello V, Croci G, Calzolari E, Bernardi F. Patracchini P, et al. Among authors: bernardi f. Hum Genet. 1992 Nov;90(3):297-8. doi: 10.1007/BF00220083. Hum Genet. 1992. PMID: 1487245

3

Detection of two missense mutations and characterization of a repeat polymorphism in the factor VII gene (F7).

Marchetti G, Patracchini P, Gemmati D, DeRosa V, Pinotti M, Rodorigo G, Casonato A, Girolami A, Bernardi F. Marchetti G, et al. Among authors: bernardi f. Hum Genet. 1992 Jul;89(5):497-502. doi: 10.1007/BF00219173. Hum Genet. 1992. PMID: 1634227

4

PCR detection of a repeat polymorphism within the F7 gene.

Marchetti G, Gemmati D, Patracchini P, Pinotti M, Bernardi F. Marchetti G, et al. Among authors: bernardi f. Nucleic Acids Res. 1991 Aug 25;19(16):4570. doi: 10.1093/nar/19.16.4570-a. Nucleic Acids Res. 1991. PMID: 1886792 Free PMC article.

5

Characterization of polymorphic markers in the von Willebrand factor gene and pseudogene.

Bernardi F, Marchetti G, Casonato A, Gemmati D, Patracchini P, Legnani C, DeRosa V, Girolami A, Conconi F. Bernardi F, et al. Br J Haematol. 1990 Mar;74(3):282-9. doi: 10.1111/j.1365-2141.1990.tb02584.x. Br J Haematol. 1990. PMID: 1970740

6

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: bernardi f. Hematol Pathol. 1990;4(4):185-8. Hematol Pathol. 1990. PMID: 2074260

7

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. Br J Haematol. 1989 Feb;71(2):271-6. doi: 10.1111/j.1365-2141.1989.tb04266.x. Br J Haematol. 1989. PMID: 2493803

8

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. Blood. 1989 Jun;73(8):2123-7. Blood. 1989. PMID: 2567188 Free article.

9

Sublocalization of von Willebrand factor pseudogene to 22q11.22-q11.23 by in situ hybridization in a 46,X,t(X;22)(pter;q11.21) translocation.

Patracchini P, Calzolari E, Aiello V, Palazzi P, Banin P, Marchetti G, Bernardi F. Patracchini P, et al. Among authors: bernardi f. Hum Genet. 1989 Oct;83(3):264-6. doi: 10.1007/BF00285168. Hum Genet. 1989. PMID: 2793170

10

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. Hum Genet. 1988 Apr;78(4):359-62. doi: 10.1007/BF00291736. Hum Genet. 1988. PMID: 2896159

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