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    Heterozygous Deletion of the 3' Portion of Factor X Gene in a Family with Factor X Deficiency.

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    Heterozygous Deletion found in the 3' Portion of Factor X Gene in a family with Coagulation Factor X Deficiency

    PCR and specific oligonucleotide hybridization for the molecular characterization and carrier detection of hemophilia A.

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    One of the first mutation detection in Haemophilia patients by PCR and ASO-probe hybridization. Translational applications for diagnostic purposes
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