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Estudi de coagulopaties congènites
Diagnosis of congenital coagulopathies by NGS molecular: Factor II Deficiency
Code:
70803
Molecular diagnosis of congenital coagulopathies by NGS: Factor V Deficiency
Code:
70804
Molecular diagnosis of congenital coagulopathies by NGS: Factor VII Deficiency
Code:
70805
Molecular Diagnosis of Congenital Coagulopathies by NGS: Factor X Deficiency
Code:
70806
Molecular Diagnosis of Congenital Coagulopathies by NGS: Factor XI Deficiency
Code:
70807
Molecular diagnosis of congenital coagulopathies by NGS: Factor XII Deficiency
Code:
70808
Molecular Diagnosis of Congenital Coagulopathies by NGS: Factor XIII Deficiency
Code:
70809
Molecular diagnosis of congenital coagulopathies by NGS: Fibrinogen Deficiency
Code:
70810
Molecular diagnosis of congenital coagulopathies by NGS: Combined Deficiency of Factor V and Factor XIII
Code:
70802
Molecular Diagnosis of Congenital Coagulopathies by NGS: Plasminogen Deficiency
Code:
70811
Molecular Diagnosis of Congenital Coagulopathies by NGS: Hemophilia A
Code:
70801
Molecular diagnosis of hemophilia B
Code:
70800
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