Haemophilia and thrombophilia: What do we learn about combined inheritance of both genetic variations?

Hamostaseologie

Volumn 23, Issue 1, 2003, Pages 36-40

  Nowak Gottl U ^a,f   Escuriola, C ^b   Kurnik, K ^c   Schobess, R ^d   Horneff, S ^d   Kosch, A ^a   Kreuz, W ^b   Pollmann, H ^e  

^a UNIVERSITY HOSPITAL MÜNSTER   (Germany)

^b UNIVERSITY HOSPITAL FRANKFURT   (Germany)

^c LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

^d MARTIN LUTHER UNIVERSITÄT HALLE WITTENBERG   (Germany)

^e Inst for Thrombosis and Haemostasis   (Germany)

^f UNIVERSITY OF MÜNSTER   (Germany)

Author keywords

Factor II G20210A; Factor V G1691A; Pediatric PUP patients; Severe haemophilia A

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); ANTITHROMBIN; BLOOD CLOTTING FACTOR 5; BLOOD CLOTTING FACTOR 8; BLOOD CLOTTING FACTOR 8 CONCENTRATE; LIPOPROTEIN A; PROTEIN C; PROTEIN S; PROTHROMBIN;

CATHETERIZATION; CHILD; CLINICAL TRIAL; COHORT ANALYSIS; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; DISEASE SEVERITY; FEMALE; GENETIC VARIABILITY; GENOTYPE; GERMANY; HEMOPHILIA; HUMAN; INHERITANCE; MAJOR CLINICAL STUDY; MALE; MULTICENTER STUDY; PHENOTYPE; PREVALENCE; PROTEIN C DEFICIENCY; REVIEW; RISK FACTOR; THROMBOPHILIA;

EID: 0037313997     PISSN: 07209355     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0037-1619560     Document Type: Review

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