Bernardi F - Search Results

1

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

2

Reduced levels of variant alpha-globins in beta-thalassaemia.

del Senno L, Bernardi F, Bruno MR, Buzzoni D, Casoni I, Marchetti G, Mariuzzi Alberti R, Perrotta CM, Conconi F. del Senno L, et al. Among authors: bernardi f. Haematologica. 1979 Jun;64(3):278-87. Haematologica. 1979. PMID: 113296 No abstract available.

3

Localization of cloned human DNA sequences and analysis of chromosomal alterations by in situ hybridization.

Patracchini P, Aiello V, Marchetti G, Palazzi P, Ferrati M, Calzolari E, Bernardi F. Patracchini P, et al. Among authors: bernardi f. Liver. 1992 Aug;12(4 Pt 2):280-5. doi: 10.1111/j.1600-0676.1992.tb01061.x. Liver. 1992. PMID: 1447960

4

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

5

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

6

Rapid detection of a protein C gene mutation present in the asymptomatic and not in the thrombosis-prone lineage.

Bernardi F, Patracchini P, Gemmati D, Boninsegna S, Guerra S, Legnani C, Ballerini G, Marchetti G. Bernardi F, et al. Br J Haematol. 1992 Jun;81(2):277-82. doi: 10.1111/j.1365-2141.1992.tb08220.x. Br J Haematol. 1992. PMID: 1643025

7

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.

8

A de novo and heterozygous gene deletion causing a variant of von Willebrand disease.

Bernardi F, Marchetti G, Guerra S, Casonato A, Gemmati D, Patracchini P, Ballerini G, Conconi F. Bernardi F, et al. Blood. 1990 Feb 1;75(3):677-83. Blood. 1990. PMID: 1967540 Free article.

9

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: bernardi f. Br J Haematol. 1991 May;78(1):71-9. doi: 10.1111/j.1365-2141.1991.tb04385.x. Br J Haematol. 1991. PMID: 2043485

10

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

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