Test Catalog

Estudi de coagulopaties congènites

Diagnosis of congenital coagulopathies by NGS: von Willebrand Disease Code: 70812
Molecular Diagnosis of Congenital Coagulopathies by NGS: Thrombotic Thrombocytopenic Purpura Code: 70813
Molecular Diagnosis of Congenital Coagulopathies by NGS: Bernard-Soulier Syndrome Code: 70814
Molecular Diagnosis of Congenital Coagulopathies by NGS: Glanzmann Thrombasthenia Code: 70815
Family study of congenital coagulopathies Code: 70816
Prenatal Study of Congenital Coagulopathies Code: 70817
Complete Exome Code: 70818
Exome Complete: Noonan Syndrome and RASopathies Code: 70832
Exome Complete: Hereditary Hemorrhagic Telangiectasia and Other Vascular Diseases Code: 70829
Exome Complete: Congenital Disorders of Glycosylation Code: 70833
Exome Complete: Hereditary Disorders of Connective Tissue Code: 70828
Exome Complete: Congenital Platelet Disorders Code: 70830