Found: 4
Select item for more details and to access through your institution.
Coinheritance of three novel FV gene mutations in a patient with a severe FV deficiency.
- Published in:
- Haemophilia, 2012, v. 18, n. 2, p. e51, doi. 10.1111/j.1365-2516.2011.02747.x
- By:
- Publication type:
- Article
Clinical histories and molecular characterization of two afibrinogenemic patients: insights into clinical management.
- Published in:
- Haemophilia, 2012, v. 18, n. 1, p. e16, doi. 10.1111/j.1365-2516.2011.02656.x
- By:
- Publication type:
- Article
Factor XI deficiency: two novel mutations in asymptomatic Italian patients.
- Published in:
- Haemophilia, 2010, v. 16, n. 5, p. 767, doi. 10.1111/j.1365-2516.2010.02241.x
- By:
- Publication type:
- Article
The M2 haplotype in the ANXA5 gene is an independent risk factor for idiopathic small-for-gestational age newborns.
- Published in:
- Molecular Human Reproduction, 2012, v. 18, n. 10, p. 510, doi. 10.1093/molehr/gas023
- By:
- Publication type:
- Article