1,720,986 research outputs found
Identificazione di mutazioni nell' Esome 24 del Gene del Fattore VIII Mediante Amplificazione Enzimatica del DNA (PCR).
Heterozygous Deletion of the 3' Portion of Factor X Gene in a Family with Factor X Deficiency.
Heterozygous Deletion found in the 3' Portion of Factor X Gene in a family with Coagulation Factor X Deficiency
MOLECULAR CHARACTERIZATION OF A PARTIAL DELETION OF VON WILLEBRAND FACTOR GENE GIVING RISE TO AN ABNORMAL PROTEIN
TECNICHE DEL DNA RICOMBINANTE APPLICATE ALLO STUDIO DELLA MALATTIA DI VON WILLEBRAND DI TIPO III E DELL'EMOFILIA A
CHROMOSOMAL MAPPING BY INSITU HYBRIDIZATION OF A FAMILY OF SEQUENCES RELATED TO GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE
PCR and specific oligonucleotide hybridization for the molecular characterization and carrier detection of hemophilia A.
One of the first mutation detection in Haemophilia patients by PCR and ASO-probe hybridization. Translational applications for diagnostic purposes
CHROMOSOMAL LOCALIZATION AND CHARACTERIZATION OF RFLPs IN THE VON WILLEBRAND FACTOR PSEUDOGENE
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