1: Scanavini D, Legnani C, Lunghi B, Mingozzi F, Palareti G, Bernardi F.
The factor VIII D1241E polymorphism is associated with decreased factor VIII activity and not with activated protein C resistance levels.
Thromb Haemost. 2005 Mar;93(3):453-6.
PMID: 15735794 [PubMed - in process]
2: Pinotti M, Bertolucci C, Portaluppi F, Colognesi I, Frigato E, Foa A, Bernardi F.
Daily and circadian rhythms of tissue factor pathway inhibitor and factor VII activity.
Arterioscler Thromb Vasc Biol. 2005 Mar;25(3):646-9. Epub 2004 Dec 16.
PMID: 15604416 [PubMed - in process]
3: Scanavini D, Girelli D, Lunghi B, Martinelli N, Legnani C, Pinotti M, Palareti G, Bernardi F.
Modulation of factor V levels in plasma by polymorphisms in the C2 domain.
Arterioscler Thromb Vasc Biol. 2004 Jan;24(1):200-6. Epub 2003 Dec 1.
PMID: 14656739 [PubMed - indexed for MEDLINE]
4: Mingozzi F, Legnani C, Lunghi B, Scanavini D, Castoldi E, Palareti G, Marchetti G, Bernardi F.
A FV multiallelic marker detects genetic components of APC resistance contributing to venous thromboembolism in FV Leiden carriers.
Thromb Haemost. 2003 Jun;89(6):983-9.
PMID: 12783110 [PubMed - indexed for MEDLINE]
5: Marchetti G, Ferraresi P, Legnani C, Pinotti M, Lunghi B, Scapoli C, Gemmati D, Coccheri S, Palareti G, Bernardi F.
Asymptomatic carriership of factor V Leiden and genotypes of the fibrinogen gene cluster.
Br J Haematol. 2003 May;121(4):632-8.
PMID: 12752105 [PubMed - indexed for MEDLINE]
6: Pinotti M, Camire RM, Baroni M, Rajab A, Marchetti G, Bernardi F.
Impaired prothrombinase activity of factor X Gly381Asp results in severe familial CRM+ FX deficiency.
Thromb Haemost. 2003 Feb;89(2):243-8.
PMID: 12574802 [PubMed - indexed for MEDLINE]
7: Toso R, Bernardi F, Tidd T, Pinotti M, Camire RM, Marchetti G, High KA, Pollak ES.
Factor VII mutant V154G models a zymogen-like form of factor VIIa.
Biochem J. 2003 Feb 1;369(Pt 3):563-71.
PMID: 12358603 [PubMed - indexed for MEDLINE]
8: Pinotti M, Marchetti G, Baroni M, Cinotti F, Morfini M, Bernardi F.
Reduced activation of the Gla19Ala FX variant via the extrinsic coagulation pathway results in symptomatic CRMred FX deficiency.
Thromb Haemost. 2002 Aug;88(2):236-41.
PMID: 12195695 [PubMed - indexed for MEDLINE]
9: Toso R, Pinotti M, High KA, Pollak ES, Bernardi F.
A frequent human coagulation Factor VII mutation (A294V, c152) in loop 140s affects the interaction with activators, tissue factor and substrates.
Biochem J. 2002 Apr 15;363(Pt 2):411-6.
PMID: 11931672 [PubMed - indexed for MEDLINE]
10: Pinotti M, Etro D, Bindini D, Papa ML, Rodorigo G, Rocino A, Mariani G, Ciavarella N, Bernardi F.
Residual factor VII activity and different hemorrhagic phenotypes in CRM(+) factor VII deficiencies (Gly331Ser and Gly283Ser).
Blood. 2002 Feb 15;99(4):1495-7. Erratum in: Blood 2001 Apr 1;99(7):2290.
Pinotti, Marko [corrected to Pinotti, Mirko]; Etro, Daniela [corrected to Etro, Daniela]; Mariani, Guglieuto [corrected to Mariani, Guglielmo].
PMID: 11830508 [PubMed - indexed for MEDLINE]
11: Castoldi E, Lunghi B, Mingozzi F, Simioni P, Girolami A, Bernardi F.
A highly polymorphic microsatellite in the factor V gene is an informative tool for the study of factor V-related disorders.
Br J Haematol. 2001 Sep;114(4):868-70.
PMID: 11564076 [PubMed - indexed for MEDLINE]
12: Kalafatis M, Simioni P, Bernardi F.
Phenotype and genotype expression in pseudohomozygous R2 factor V.
Blood. 2001 Sep 15;98(6):1988-9. No abstract available.
PMID: 11565539 [PubMed - indexed for MEDLINE]
13: Castoldi E, Simioni P, Kalafatis M, Lunghi B, Tormene D, Girelli D, Girolami A, Bernardi F.
Combinations of 4 mutations (FV R506Q, FV H1299R, FV Y1702C, PT 20210G/A) affecting the prothrombinase complex in a thrombophilic family.
Blood. 2000 Aug 15;96(4):1443-8.
PMID: 10942390 [PubMed - indexed for MEDLINE]
14: Girelli D, Russo C, Ferraresi P, Olivieri O, Pinotti M, Friso S, Manzato F, Mazzucco A, Bernardi F, Corrocher R.
Polymorphisms in the factor VII gene and the risk of myocardial infarction in patients with coronary artery disease.
N Engl J Med. 2000 Sep 14;343(11):774-80.
PMID: 10984565 [PubMed - indexed for MEDLINE]
15: Pinotti M, Toso R, Girelli D, Bindini D, Ferraresi P, Papa ML, Corrocher R, Marchetti G, Bernardi F.
Modulation of factor VII levels by intron 7 polymorphisms: population and in vitro studies.
Blood. 2000 Jun 1;95(11):3423-8.
PMID: 10828024 [PubMed - indexed for MEDLINE]
16: Gandrille S, Borgel D, Sala N, Espinosa-Parrilla Y, Simmonds R, Rezende S, Lind B, Mannhalter C, Pabinger I, Reitsma PH, Formstone C, Cooper DN, Saito H, Suzuki K, Bernardi F, Aiach M; Plasma Coagulation Inhibitors Subcommittee of the
Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis.
Protein S deficiency: a database of mutations--summary of the first update.
Thromb Haemost. 2000 Nov;84(5):918. No abstract available.
PMID: 11127877 [PubMed - indexed for MEDLINE]
17: Grifa A, Wagner CA, D'Ambrosio L, Melchionda S, Bernardi F, Lopez-Bigas N, Rabionet R, Arbones M, Monica MD, Estivill X, Zelante L, Lang F, Gasparini P.
Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus.
Nat Genet. 1999 Sep;23(1):16-8. No abstract available.
PMID: 10471490 [PubMed - indexed for MEDLINE]
18: Kalafatis M, Bernardi F, Simioni P, Lunghi B, Girolami A, Mann KG.
Phenotype and genotype expression in pseudohomozygous factor VLEIDEN : the need for phenotype analysis.
Arterioscler Thromb Vasc Biol. 1999 Feb;19(2):336-42.
PMID: 9974416 [PubMed - indexed for MEDLINE]
19: Bernardi F, Casonato A, Marchetti G, Gemmati D, Bizzaro N, Pontara E, Girolami A.
Two novel mutations (Pro864His, Val867Glu) causing type 2A von Willebrand disease and affecting a single restriction site in exon 28.
Br J Haematol. 1998 Dec;103(3):885-7.
PMID: 9858250 [PubMed - indexed for MEDLINE]
20: Castoldi E, Kalafatis M, Lunghi B, Simioni P, Ioannou PA, Petio M, Girolami A, Mann KG, Bernardi F.
Molecular bases of pseudo-homozygous APC resistance: the compound heterozygosity for FV R506Q and a FV null mutation results in the exclusive presence of FV Leiden molecules in plasma.
Thromb Haemost. 1998 Sep;80(3):403-6.
PMID: 9759618 [PubMed - indexed for MEDLINE]
21: Pinotti M, Toso R, Redaelli R, Berrettini M, Marchetti G, Bernardi F.
Molecular mechanisms of FVII deficiency: expression of mutations clustered in the IVS7 donor splice site of factor VII gene.
Blood. 1998 Sep 1;92(5):1646-51.
PMID: 9716592 [PubMed - indexed for MEDLINE]
22: Rosendaal FR, Doggen CJ, Zivelin A, Arruda VR, Aiach M, Siscovick DS, Hillarp A, Watzke HH, Bernardi F, Cumming AM, Preston FE, Reitsma PH. Related Articles, Links
Geographic distribution of the 20210 G to A prothrombin variant.
Thromb Haemost. 1998 Apr;79(4):706-8.
PMID: 9569177 [PubMed - indexed for MEDLINE]
23: Bernardi F, Arcieri P, Bertina RM, Chiarotti F, Corral J, Pinotti M, Prydz H, Samama M, Sandset PM, Strom R, Garcia VV, Mariani G.
Contribution of factor VII genotype to activated FVII levels. Differences in genotype frequencies between northern and southern European populations.
Arterioscler Thromb Vasc Biol. 1997 Nov;17(11):2548-53.
PMID: 9409226 [PubMed - indexed for MEDLINE]
24: Gandrille S, Borgel D, Ireland H, Lane DA, Simmonds R, Reitsma PH, Mannhalter C, Pabinger I, Saito H, Suzuki K, Formstone C, Cooper DN, Espinosa Y, Sala N, Bernardi F, Aiach M.
Protein S deficiency: a database of mutations. For the Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis.
Thromb Haemost. 1997 Jun;77(6):1201-14. No abstract available.
PMID: 9241758 [PubMed - indexed for MEDLINE]
25: Ferraresi P, Marchetti G, Legnani C, Cavallari E, Castoldi E, Mascoli F, Ardissino D, Palareti G, Bernardi F.
The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease.
Arterioscler Thromb Vasc Biol. 1997 Nov;17(11):2418-22.
PMID: 9409210 [PubMed - indexed for MEDLINE]
26: Castoldi E, Lunghi B, Mingozzi F, Ioannou P, Marchetti G, Bernardi F.
New coagulation factor V gene polymorphisms define a single and infrequent haplotype underlying the factor V Leiden mutation in Mediterranean populations and Indians.
Thromb Haemost. 1997 Sep;78(3):1037-41.
PMID: 9308750 [PubMed - indexed for MEDLINE]
27: Bernardi F, Faioni EM, Castoldi E, Lunghi B, Castaman G, Sacchi E, Mannucci PM.
A factor V genetic component differing from factor V R506Q contributes to the activated protein C resistance phenotype.
Blood. 1997 Aug 15;90(4):1552-7.
PMID: 9269773 [PubMed - indexed for MEDLINE]
28: Bernardi F, Legnani C, Micheletti F, Lunghi B, Ferraresi P, Palareti G, Biagi R, Marchetti G.
A heparin cofactor II mutation (HCII Rimini) combined with factor V Leiden or type I protein C deficiency in two unrelated thrombophilic subjects.
Thromb Haemost. 1996 Oct;76(4):505-9.
PMID: 8902986 [PubMed - indexed for MEDLINE]
29: Bernardi F, Castaman G, Pinotti M, Ferraresi P, Di Iasio MG, Lunghi B, Rodeghiero F, Marchetti G.
Mutation pattern in clinically asymptomatic coagulation factor VII deficiency.
Hum Mutat. 1996;8(2):108-15.
PMID: 8844208 [PubMed - indexed for MEDLINE]
30: Lunghi B, Iacoviello L, Gemmati D, Dilasio MG, Castoldi E, Pinotti M, Castaman G, Redaelli R, Mariani G, Marchetti G, Bernardi F.
Detection of new polymorphic markers in the factor V gene: association with factor V levels in plasma.
Thromb Haemost. 1996 Jan;75(1):45-8.
PMID: 8713778 [PubMed - indexed for MEDLINE]
31: Gemmati D, Serino ML, Moratelli S, Ballerini G, Furbetta M, Lunghi B, Marchetti G, Bernardi F.
A novel mutation (Leu817Pro) causing type 2A von Willebrand disease.
Br J Haematol. 1996 Jan;92(1):241-3.
PMID: 8562403 [PubMed - indexed for MEDLINE]
32: Bernardi F, Marchetti G, Pinotti M, Arcieri P, Baroncini C, Papacchini M, Zepponi E, Ursicino N, Chiarotti F, Mariani G.
Factor VII gene polymorphisms contribute about one third of the factor VII level variation in plasma.
Arterioscler Thromb Vasc Biol. 1996 Jan;16(1):72-6.
PMID: 8548429 [PubMed - indexed for MEDLINE]
33: Marchetti G, Castaman G, Pinotti M, Lunghi B, Di Iasio MG, Ruggieri M, Rodeghiero F, Bernardi F.
Molecular bases of CRM+ factor X deficiency: a frequent mutation (Ser334Pro) in the catalytic domain and a substitution (Glu102Lys) in the second EGF-like domain.
Br J Haematol. 1995 Aug;90(4):910-5.
PMID: 7669671 [PubMed - indexed for MEDLINE]
34: Formstone CJ, Wacey AI, Berg LP, Rahman S, Bevan D, Rowley M, Voke J, Bernardi F, Legnani C, Simioni P, Girolami A, Tuddenham EG, Kakkar VV, Cooper DN.
Detection and characterization of seven novel protein S (PROS) gene lesions: evaluation of reverse transcript-polymerase chain reaction as a mutation screening strategy.
Blood. 1995 Oct 1;86(7):2632-41.
PMID: 7545463 [PubMed - indexed for MEDLINE]
35: Reitsma PH, Bernardi F, Doig RG, Gandrille S, Greengard JS, Ireland H, Krawczak M, Lind B, Long GL, Poort SR, et al.
Protein C deficiency: a database of mutations, 1995 update. On behalf of the Subcommittee on Plasma Coagulation Inhibitors of the Scientific and Standardization Committee of the ISTH.
Thromb Haemost. 1995 May;73(5):876-89. Review. No abstract available.
PMID: 7482420 [PubMed - indexed for MEDLINE]
36: Bernardi F, Castaman G, Redaelli R, Pinotti M, Lunghi B, Rodeghiero F, Marchetti G.
Topologically equivalent mutations causing dysfunctional coagulation factors VII (294Ala-->Val) and X (334Ser-->Pro).
Hum Mol Genet. 1994 Jul;3(7):1175-7. No abstract available.
PMID: 7981691 [PubMed - indexed for MEDLINE]
37: Bernardi F, Liney DL, Patracchini P, Gemmati D, Legnani C, Arcieri P, Pinotti M, Redaelli R, Ballerini G, Pemberton S, et al.
Molecular defects in CRM+ factor VII deficiencies: modelling of missense mutations in the catalytic domain of FVII.
Br J Haematol. 1994 Mar;86(3):610-8.
PMID: 8043443 [PubMed - indexed for MEDLINE]
38: Bernardi F, Patracchini P, Gemmati D, Ferrati M, Arcieri P, Papacchini M, Redaelli R, Baudo F, Mariani G, Marchetti G.
Molecular analysis of factor VII deficiency in Italy: a frequent mutation (FVII Lazio) in a repeated intronic region.
Hum Genet. 1993 Nov;92(5):446-50.
PMID: 8244334 [PubMed - indexed for MEDLINE]
39: Marchetti G, Legnani C, Patracchini P, Gemmati D, Ferrati M, Palareti G, Coccheri S, Bernardi F.
Study of a protein S gene polymorphism at DNA and mRNA level in a family with symptomatic protein S deficiency.
Br J Haematol. 1993 Sep;85(1):173-5.
PMID: 7902733 [PubMed - indexed for MEDLINE]
40: Reitsma PH, Poort SR, Bernardi F, Gandrille S, Long GL, Sala N, Cooper DN.
Protein C deficiency: a database of mutations. For the Protein C & S Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis.
Thromb Haemost. 1993 Jan 11;69(1):77-84. Review. No abstract available.
PMID: 8446940 [PubMed - indexed for MEDLINE]
41: Marchetti G, Ferrati M, Patracchini P, Redaelli R, Bernardi F.
A missense mutation (178Cys-->Tyr) and two neutral dimorphisms (115His and 333Ser) in the human coagulation factor VII gene.
Hum Mol Genet. 1993 Jul;2(7):1055-6. No abstract available.
PMID: 8364544 [PubMed - indexed for MEDLINE]
42: Marchetti G, Patracchini P, Gemmati D, Castaman G, Rodeghiero F, Wacey A, Cooper DN, Tuddenham EG, Bernardi F.
Symptomatic type II protein C deficiency caused by a missense mutation (Gly 381-->Ser) in the substrate-binding pocket.
Br J Haematol. 1993 Jun;84(2):285-9.
PMID: 8398832 [PubMed - indexed for MEDLINE]
43: Bernardi F, Patracchini P, Gemmati D, Pinotti M, Schwienbacher C, Ballerini G, Marchetti G.
In-frame deletion of von Willebrand factor A domains in a dominant type of von Willebrand disease.
Hum Mol Genet. 1993 May;2(5):545-8.
PMID: 8518792 [PubMed - indexed for MEDLINE]
44: Marchetti G, Patracchini P, Papacchini M, Ferrati M, Bernardi F.
A polymorphism in the 5' region of coagulation factor VII gene (F7) caused by an inserted decanucleotide.
Hum Genet. 1993 Jan;90(5):575-6.
PMID: 8381388 [PubMed - indexed for MEDLINE]
45: Patracchini P, Marchetti G, Aiello V, Croci G, Calzolari E, Bernardi F.
Characterization and mapping of the 5' portion of von Willebrand factor pseudogene.
Hum Genet. 1992 Nov;90(3):297-8.
PMID: 1487245 [PubMed - indexed for MEDLINE]
46: Marchetti G, Patracchini P, Gemmati D, DeRosa V, Pinotti M, Rodorigo G, Casonato A, Girolami A, Bernardi F.
Detection of two missense mutations and characterization of a repeat polymorphism in the factor VII gene (F7).
Hum Genet. 1992 Jul;89(5):497-502.
PMID: 1634227 [PubMed - indexed for MEDLINE]
47: Bernardi F, Patracchini P, Gemmati D, Boninsegna S, Guerra S, Legnani C, Ballerini G, Marchetti G.
Rapid detection of a protein C gene mutation present in the asymptomatic and not in the thrombosis-prone lineage.
Br J Haematol. 1992 Jun;81(2):277-82.
PMID: 1643025 [PubMed - indexed for MEDLINE]
48: Marchetti G, Gemmati D, Patracchini P, Pinotti M, Bernardi F.
PCR detection of a repeat polymorphism within the F7 gene.
Nucleic Acids Res. 1991 Aug 25;19(16):4570. No abstract available.
PMID: 1886792 [PubMed - indexed for MEDLINE]
49: Marchetti G, Patracchini P, Volinia S, Aiello V, Schiavoni M, Ciavarella N, Calzolari E, Schwienbacher C, Bernardi F.
Characterization of the pseudogenic and genic homologous regions of von Willebrand factor.
Br J Haematol. 1991 May;78(1):71-9.
PMID: 2043485 [PubMed - indexed for MEDLINE]
50: Bernardi F, Marchetti G, Casonato A, Gemmati D, Patracchini P, Legnani C, DeRosa V, Girolami A, Conconi F.
Characterization of polymorphic markers in the von Willebrand factor gene and pseudogene.
Br J Haematol. 1990 Mar;74(3):282-9.
PMID: 1970740 [PubMed - indexed for MEDLINE]
51: Bernardi F, Marchetti G, Guerra S, Casonato A, Gemmati D, Patracchini P, Ballerini G, Conconi F.
A de novo and heterozygous gene deletion causing a variant of von Willebrand disease.
Blood. 1990 Feb 1;75(3):677-83.
PMID: 1967540 [PubMed - indexed for MEDLINE]
52: Marchetti G, Gemmati D, Patracchini P, Volinia S, Castagnoli A, Tosi B, Capelli M, Bernardi F.
Direct detection of a missense mutation causing severe hemophilia A by PCR amplification and fluorescence scanning.
Hematol Pathol. 1990;4(4):185-8.
PMID: 2074260 [PubMed - indexed for MEDLINE]
53: Patracchini P, Calzolari E, Aiello V, Palazzi P, Banin P, Marchetti G, Bernardi F.
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.
Hum Genet. 1989 Oct;83(3):264-6.
PMID: 2793170 [PubMed - indexed for MEDLINE]
54: Bernardi F, Marchetti G, Patracchini P, Volinia S, Gemmati D, Simioni P, Girolami A.
Partial gene deletion in a family with factor X deficiency.
Blood. 1989 Jun;73(8):2123-7.
PMID: 2567188 [PubMed - indexed for MEDLINE]
55: Marchetti G, Sacchi E, Patracchini P, Randi AM, Sampietro M, Bernardi F.
Two additional TaqI RFLPs in von Willebrand factor gene (VWF) and pseudogene.
Nucleic Acids Res. 1989 Apr 25;17(8):3329. No abstract available.
PMID: 2566970 [PubMed - indexed for MEDLINE]
56: Volinia S, Gambari R, Bernardi F, Barrai I.
The frequency of oligonucleotides in mammalian genic regions.
Comput Appl Biosci. 1989 Feb;5(1):33-40.
PMID: 2924169 [PubMed - indexed for MEDLINE]
57: Bernardi F, Volinia S, Patracchini P, Gemmati D, Boninsegna S, Schwienbacher C, Marchetti G.
A recurrent missense mutation (Arg----Gln) and a partial deletion in factor VIII gene causing severe haemophilia A.
Br J Haematol. 1989 Feb;71(2):271-6.
PMID: 2493803 [PubMed - indexed for MEDLINE]
58: Patracchini P, Aiello V, Palazzi P, Calzolari E, Bernardi F.
Sublocalization of the human protein C gene on chromosome 2q13-q14.
Hum Genet. 1989 Jan;81(2):191-2.
PMID: 2912888 [PubMed - indexed for MEDLINE]
59: Bernardi F, Marchetti G, Volinia S, Patracchini P, Casonato A, Girolami A, Conconi F.
A frequent factor XII gene mutation in Hageman trait.
Hum Genet. 1988 Oct;80(2):149-51.
PMID: 3169737 [PubMed - indexed for MEDLINE]
60: Volinia S, Bernardi F, Gambari R, Barrai I.
Co-localization of rare oligonucleotides and regulatory elements in mammalian upstream gene regions.
J Mol Biol. 1988 Sep 20;203(2):385-90.
PMID: 3199439 [PubMed - indexed for MEDLINE]
61: Bernardi F, Legnani C, Volinia S, Patracchini P, Rodorigo G, DeRosa V, Marchetti G.
A HindIII RFLP and a gene lesion in the coagulation factor VIII gene.
Hum Genet. 1988 Apr;78(4):359-62.
PMID: 2896159 [PubMed - indexed for MEDLINE]
62: Bernardi F, Guerra S, Patracchini P, Volinia S, Buzzoni D, Ballerini G, Casonato A, Marchetti G.
von Willebrand disease investigated by two novel RFLPs.
Br J Haematol. 1988 Feb;68(2):243-8.
PMID: 2894837 [PubMed - indexed for MEDLINE]
63: Bernardi F, del Senno L, Barbieri R, Buzzoni D, Gambari R, Marchetti G, Conconi F, Panicucci F, Positano M, Pitruzzello
Gene deletion in an Italian haemophilia B subject.
J Med Genet. 1985 Aug;22(4):305-7.
PMID: 4045960 [PubMed - indexed for MEDLINE]
64: Del Senno L, Bernardi F, Buzzoni D, Casoni I, Marchetti G, Perrotta C, Conconi F, Cristofori G, Salsini G, Vullo C, Cappellozza G, Bellinello F, Bedendo B, Mercuriati M.
alpha-Thalassemia trait in the region of Ferrara.
Haematologica. 1981 Apr;66(2):181-6. No abstract available.
PMID: 6791994 [PubMed - indexed for MEDLINE]
65: del Senno L, Bernardi F, Marchetti G, Perrotta C, Conconi F, Vullo C, Salsini G, Cristofori G, Cappellozza G, Bellinello F, Bedendo B, Mercuriati M.
Organization of alpha-globin genes and mRNA translation in subjects carrying haemoglobin Hasharon (alpha 47 Asp replaced by His) from the Ferrara Region (Northern Italy).
Eur J Biochem. 1980 Oct;111(1):125-30.
PMID: 6254772 [PubMed - indexed for MEDLINE]
66: Conconi F, Bernardi F, Buzzoni D, Casoni I, del Senno L, Marchetti G, Perrotta CM.
beta-Globin messenger RNA in Ferrara beta 0 thalassemia.
Ann N Y Acad Sci. 1980;344:120-31. No abstract available.
PMID: 6930863 [PubMed - indexed for MEDLINE]