Prenatal diagnosis of haemophilia B: the Italian experience-Reference-Cited by-同舟云学术

Prenatal diagnosis of haemophilia B: the Italian experience

Published:2013-06-28 Issue:6 Volume:19 Page:898-903
ISSN:1351-8216
Container-title:Haemophilia
language:en
Short-container-title:Haemophilia

Author:

Belvini D.¹,Salviato R.¹,Acquila M.²,Bicocchi M. P.²,Frusconi S.³,Garagiola I.⁴,Sanna V.⁵,Santacroce R.⁶,Rocino A.⁷,Tagariello G.¹

Affiliation:

1. Dipartimento di Laboratorio, Servizio Trasfusionale; Centro per le Malattie del Sangue e Presidio Regionale Malattie rare per le Coagulopatie Congenite; Castelfranco Veneto Hospital (TV); Castelfranco Veneto Italy

2. Laboratorio di Ematologia ed Emofilia; IV Divisione di Pediatria; Istituto Gaslini; Genova Italy

3. SOD Diagnostica Genetica; Centro Regionale Riferimento Coagulopatie Congenite; Azienda Ospedaliero-Universitaria Careggi; Firenze Italy

4. U.O.S. Dipartimentale per la Diagnosi e la terapia delle Coagulopatie; Angelo Bianchi Bonomi Hemophilia and Thrombosis Center; Fondazione IRCCS Ca' Granda-Ospedale Maggiore Policlinico; Università di Milano; Milano Italy

5. Dipartimento di Biochimica e mediche; Universitdi Napoli ‘Federico II’; CEINGE-Biotecnologie Avanzate; Napoli Italy

6. Istituto di Genetica Medica, Dipartimento di Scienze Biomediche; Universitdi Foggia; Foggia Italy

7. Centro Emofilia e Trombosi; Ospedale S.Giovanni Bosco; Napoli Italy

Publisher

Wiley

Subject

Genetics (clinical),Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/hae.12219/fullpdf

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4. Haemophilia A and haemophilia B: molecular insights;Bowen;Mol Pathol,2002

5. Mutation analysis of haemophilia B in the Irish population: increased prevalence caused by founder effect;Jenkins;Haemophilia,2008

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