## Abstract The first reported case of clinically significant congenital Factor VII deficiency in association with the 13q deletion syndrome is presented. It illustrates the importance of knowledge of the specific genes involved in gross deletion syndromes and adds to the current clinical experienc
β¦ LIBER β¦
Secondary severe factor X deficiency associated with antiphospholipid syndrome
β Scribed by P. Mishra; T. Chatterjee; A. Dixit; V.P. Choudhry; Rajat Kumar; R. Saxena
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 84 KB
- Volume
- 76
- Category
- Article
- ISSN
- 0361-8609
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