THE INHERITANCE OF STUART DISEASE-Reference-Cited by-同舟云学术

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THE INHERITANCE OF STUART DISEASE

Published:1965-03 Issue:3 Volume:249 Page:291-294
ISSN:0002-9629
Container-title:The American Journal of the Medical Sciences
language:en
Short-container-title:The American Journal of the Medical Sciences

Author:

Lechler Eckhard,Webster William P.,Roberts Harold R.,Penick George D.

Publisher

Elsevier BV

Subject

General Medicine

Cited by 20 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Congenital Haemorrhagic Condition Similar but Not Identical to Factor X Deficiency;Scandinavian Journal of Haematology;2009-04-24

2. Use of Prothrombin Complex Concentrates for Prophylaxis and Treatment of Bleeding Episodes in Patients with Hereditary Deficiency of Prothrombin, Factor VII, Factor X, Protein C, Protein S, or Protein Z;Thrombosis Research;1999-08

3. Liver-specific expression of the gene coding for human factor X, a blood coagulation factor.;Journal of Biological Chemistry;1992-04

4. Neonatal Congenital Factor X Deficiency;Pediatric Hematology and Oncology;1991-01

5. Der spontane Quickwert von „50%“;16. Hämophilie-Symposion;1987

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