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Screening for mutations in factor VIII gene using the single-strand conformation polymorphism.
Hum Mutat. 1995;5(4):357-9. doi: 10.1002/humu.1380050418.
Hum Mutat. 1995.
PMID: 7627196
No abstract available.
Behçet syndrome associated with protein S deficiency.
Chafa O, Fischer AM, Meriane F, Chellali T, Sternberg C, Otmani F, Benabadji M.
Chafa O, et al. Among authors: chellali t.
Thromb Haemost. 1992 Jan 23;67(1):1-3.
Thromb Haemost. 1992.
PMID: 1535461
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Severe hypofibrinogenemia associated with bilateral ischemic necrosis of toes and fingers.
Chafa O, Chellali T, Sternberg C, Reghis A, Hamladji RM, Fischer AM.
Chafa O, et al. Among authors: chellali t.
Blood Coagul Fibrinolysis. 1995 Sep;6(6):549-52. doi: 10.1097/00001721-199509000-00008.
Blood Coagul Fibrinolysis. 1995.
PMID: 7578897
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