Kaser EG: Genotyp-Phänotyp-Korrelation beim leichten hereditären ...

86
Rost S, Fregin A, Ivaskevicius V, Conzelmann E, Hörtnagel K, Pelz HJ, Lappegard K,
Seifried E, Scharrer I, Tuddenham EG, Müller CR, Strom TM, Oldenburg J. Mutations in
VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2.
Nature 2004; 427: 537−541
Rott H, Kappert G, Halimeh S, Trobisch H, 2007: Normal values for factor VII activity in
normal pregnancy and in pregnancy of women with congenital factor VII-deficiency.
http://www.gzrr.de/assets/files/Publikationen/Publikationen%202007/2007_07PostVIISS
NWgenfrott.pdf (Zugriffsdatum 30.08.2011)
Saiki RK, Gelfand DH, Stoffel S, Scharf SJ, Higuchi R, Horn GT, Mullis KB, Erlich HA.
Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase:
Science 1988; 239: 487−491
Sambrook J, Russell DW. Detection of DNA in agarose gels; adapted protocol. In:
Molecular Cloning. New York: Cold Spring Harbor, 2001
Scharrer I. Women with von Willebrand disease. Hämostaseologie 2004; 24: 44–9
The International HapMap Consortium: The International HapMap Project. In: Nature
Publishing Group 2003; 426: 789−796
Temple A, Luong LA, Cruickshank K, Humphries SE. The 10-base-pair insertion in the
promoter of the factor VII gene is not associated with lower levels of factor VIIc in
Afrocaribeans. Thromb Haemost. 1997; 77: 213−214
Thomas L. Labor und Diagnose, Indikation und Bewertung von Laborbefunden für die
medizinische Diagnostik. Marburg: Die Medizinische Verlagsgesellschaft Marburg, 1988
Tuddenham EGD, Pemberton S, Cooper DN. Inherited factor VII deficiency: genetics
and molecular pathology. Thrombosis and Haemostasis 1995; 74: 313−321
Voet D, Voet JG. Biochemie. Weinheim: Wiley-VCH Verlag, 1994