Rare Bleeding Disorder Registry: deficiencies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1538-7836.2003.t01-1-00553.x/fullpdf
Reference36 articles.
1. 1 EGD Tuddenham, and DN. Cooper In: The Molecular Genetics of Haemostasis and its Inherited Disorders. Oxford Monographs on Medical Genetics No. 25. Oxford: Oxford Medical Publications, 1994 : 112 -33 .
2. Inheritance and bleeding in factor XI deficiency
3. Rarer Quantitative and Qualitative Abnormalities of Coagulation
4. Identification and Three-dimensional Structural Analysis of Nine Novel Mutations in Patients with Prothrombin Deficiency
5. Familial Coagulation Factor V Deficiency Caused by a Novel 4 Base Pair Insertion in the Factor V Gene: Factor V Stanford
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