Large deletions identified in patients with von Willebrand disease using multiple ligation-dependent probe amplification
PMID: 21410641
Gene: VWF
HGNCID: 12726
2 Matching Annotations
- Oct 2026
-
www.jthjournal.org www.jthjournal.org
-
-
pmc.ncbi.nlm.nih.gov pmc.ncbi.nlm.nih.gov
-
Clinical, Phenotypic and Genotypic Characteristics of Von Willebrand Disease in Afro-Caribbeans: Results From a Study in Martinique Island, French West Indies
PMID: 40123275
Gene: VWF
HGNCID: 12726
-