Congenital dysfibrinogenemias: molecular abnormalities of fibrinogen
- PMID: 990483
- DOI: 10.1007/BF00995218
Congenital dysfibrinogenemias: molecular abnormalities of fibrinogen
Similar articles
-
[Congenital dysfibrinogenemia. Apropos of 13 cases].Sem Hop. 1983 Oct 13;59(36):2517-23. Sem Hop. 1983. PMID: 6316508 French.
-
[Fibrinogen "Hannover", a further abnormal fibrinogen].Blut. 1977 Feb;34(2):99-106. doi: 10.1007/BF00999856. Blut. 1977. PMID: 836970 German.
-
[Study of acquired dysfibrinogenemias. I. Importance of the comparative study of 2 methods of determination of fibrinogen for the demonstration of dysfibrinogenemias].Stud Cercet Med Interna. 1969;10(6):525-35. Stud Cercet Med Interna. 1969. PMID: 5370609 Romanian. No abstract available.
-
Abnormal fibrinogens. A review.Thromb Diath Haemorrh. 1973 Jun 28;29(3):525-35. Thromb Diath Haemorrh. 1973. PMID: 4586807 Review. No abstract available.
-
[Fibrinogen (factor I) and dys (functional) -fibrinogen].Nihon Rinsho. 2004 Dec;62 Suppl 12:597-9. Nihon Rinsho. 2004. PMID: 15658399 Review. Japanese. No abstract available.
Cited by
-
Fibrinogen gamma chain locus is on chromosome 4 in man.Hum Genet. 1982;61(1):24-6. doi: 10.1007/BF00291325. Hum Genet. 1982. PMID: 6957371
References
MeSH terms
Substances
LinkOut - more resources
Other Literature Sources