Found: 9
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Identification of 217 unreported mutations in the F8 gene in a group of 1,410 unselected Italian patients with hemophilia A.
- Published in:
- Journal of Human Genetics, 2008, v. 53, n. 3, p. 275, doi. 10.1007/s10038-007-0238-y
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- Publication type:
- Article
Multiplex ligation-dependent probe amplification as first mutation screening for large deletions and duplications in haemophilia.
- Published in:
- Haemophilia, 2017, v. 23, n. 2, p. e124, doi. 10.1111/hae.13143
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- Publication type:
- Article
Prenatal diagnosis of haemophilia B: the Italian experience.
- Published in:
- Haemophilia, 2013, v. 19, n. 6, p. 898, doi. 10.1111/hae.12219
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- Publication type:
- Article
Prenatal diagnosis of haemophilia A by using intron 1 inversion detection.
- Published in:
- 2007
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- Publication type:
- Letter
F8 gene mutation profile and ITT response in a cohort of Italian haemophilia A patients with inhibitors.
- Published in:
- Haemophilia, 2007, v. 13, n. 4, p. 361, doi. 10.1111/j.1365-2516.2007.01437.x
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- Article
LETTER TO THE EDITOR Factor VIII gene intron 1 inversion: lower than expected prevalence in Italian haemophiliac severe patients.
- Published in:
- 2004
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- Publication type:
- Letter
Hepatitis C virus quasispecies in the natural course of HCV-related disease in patients with haemophilia.
- Published in:
- Haemophilia, 2004, v. 10, n. 1, p. 81, doi. 10.1046/j.1365-2516.2003.00846.x
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- Article
Large FVIII gene deletion confers very high risk of inhibitor development in three related severe haemophiliacs.
- Published in:
- Haemophilia, 2002, v. 8, n. 1, p. 17, doi. 10.1046/j.1365-2516.2002.00578.x
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- Publication type:
- Article
Rapid prenatal diagnosis of haemophilia.
- Published in:
- Haemophilia, 2001, v. 7, n. 6, p. 603, doi. 10.1046/j.1365-2516.2001.00572.x
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- Publication type:
- Article