A Laboratory Phenotype/Genotype Correlation of 1167 French Patients From 670 Families With von Willebrand Disease A New Epidemiologic Picture
PMID: 26986123 Gene: von Willebrand factor HGNCID: 12726 Note: reported for group analysis with no associated probands/patient
Common large partial VWF gene deletion does not cause alloantibody formation in the Hungarian type 3 von Willebrand disease population
PMID: 21362127 Gene: von Willebrand factor HGNCID: 12726
The genetics of Canadian type 3 von Willebrand disease: further evidence for co-dominant inheritance of mutant alleles
PMID: 23311757 Gene: von Willebrand factor HGNCID: 12726
Alpha vs. Gamma sarcoglycanopathy: DNA tests solve a case from Argentina
PMID: 18421900
Gene: SGCA
HGNCID: 10805
National experience with adenosine deaminase deficiency related SCID in Polish children
PMID:36685585
Gene: Adenosine Deaminase (ADA)
HGNCID: 186