Simple and rapid combined genetic diagnosis of mutation (1691 G-->A) of the factor V gene and (20210 G-->A) of the prothrombin gene. | Blood Coagul Fibrinolysis;9(6): 549-51, 1998 Sep. | MEDLINE

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Simple and rapid combined genetic diagnosis of mutation (1691 G-->A) of the factor V gene and (20210 G-->A) of the prothrombin gene.

Dupérat, V G; Fauchon, M; Nurden, A T; Vergnes, C.

Affiliation

Dupérat VG; CNRS UMR 5533, Hôpital Cardiologique, Pessac, France.

Blood Coagul Fibrinolysis ; 9(6): 549-51, 1998 Sep.

Article in En | MEDLINE | ID: mdl-9819006

Subject(s)

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Collection: 01-internacional Database: MEDLINE Main subject: Factor V / Prothrombin / DNA Mutational Analysis Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Blood Coagul Fibrinolysis Journal subject: ANGIOLOGIA / HEMATOLOGIA Year: 1998 Document type: Article Affiliation country: Francia Country of publication: Reino Unido

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Collection: 01-internacional Database: MEDLINE Main subject: Factor V / Prothrombin / DNA Mutational Analysis Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Blood Coagul Fibrinolysis Journal subject: ANGIOLOGIA / HEMATOLOGIA Year: 1998 Document type: Article Affiliation country: Francia Country of publication: Reino Unido