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Thromb Haemost 2002; 88(02): 370-371
DOI: 10.1055/s-0037-1613219
DOI: 10.1055/s-0037-1613219
Letters to the Editor
Perinatal Management of Patients at High Risk of Homozygous Protein C Deficiency
Further Information
Publication History
Received
26 February 2002
Accepted
03 May 2002
Publication Date:
07 December 2017 (online)
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References
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- 3 Marlar RA, Montgomery RR, Broekmans AW. Report on the diagnosis and treatment of homozygous protein C deficiency. Report of the Working Party on Homozygous Protein C Deficiency of the ICTH-Subcommittee on Protein C and Protein S. Thromb Haemost 1989; 61 (03) 529-31.
- 4 Jerkeman A, Henriksson P, Jonsson NO, Berntorp E. [Homozygous protein C deficiency can be detected by prenatal diagnosis]. Lakartidningen 1998; 95 (36) 3772. 3775-7.
- 5 Millar DS, Allgrove J, Rodeck C, Kakkar VV, Cooper DN. A homozygous deletion/insertion mutation in the protein C (PROC) gene causing neonatal Purpura fulminans: prenatal diagnosis in an at-risk pregnancy. Blood Coagul Fibrinolysis 1994; 05 (04) 647-9.
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- 7 Reverdiau-Moalic P, Delahousse B, Body G, Bardos P, Leroy J, Gruel Y. Evolution of blood coagulation activators and inhibitors in the healthy human fetus. Blood 1996; 88 (03) 900-6.