Combination of congenital coagulation disorders: Factor II gene mutation G20210A,Factor V Leiden gene mutation G1691A and protein S deficiency. a family study期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

Combination of congenital coagulation disorders: Factor II gene mutation G20210A,Factor V Leiden gene mutation G1691A and protein S deficiency. a family study

Authors:	González Cocaño M C Díaz-Golpe V Martín S Sánchez Del Real J Redondo M C

Affiliation:	Servicio de Análisis Clínicos, Hospital de León, Spain.

Abstract:

Keywords:
本文献已被 PubMed 等数据库收录！