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1. "In vitro" correction of the severe factor V deficiency‐related coagulopathy by a novel plasma‐derived factor V concentrate. Issue 4 (26th March 2018)

2. 60. FOUR YEARS EXPERIENCE OF PREIMPLANTATION GENETIC TESTING OF FOUR MONOGENIC DISORDERS (CYSTIC FIBROSIS, BETA-THALASSAEMIA, HEMOPHILIA A AND B). (August 2019)

6. A synonymous (c.3390C>T) or a splice‐site (c.3380‐2A>G) mutation causes exon 26 skipping in four patients with von Willebrand disease (2A/IIE). Issue 7 (15th July 2013)