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- [3] CARRIER DETECTION OF HEMOPHILIA-B BY USING A RESTRICTION SITE POLYMORPHISM ASSOCIATED WITH THE COAGULATION FACTOR-IX GENE JOURNAL OF CLINICAL INVESTIGATION, 1984, 73 (05): : 1491 - 1495
- [4] HEMOPHILIA-B CAUSED BY A DELETION IN FACTOR-IX GENE JOURNAL OF CLINICAL CHEMISTRY AND CLINICAL BIOCHEMISTRY, 1987, 25 (03): : 148 - 149
- [5] SYSTEMATIC STUDY OF HEMOPHILIA-B IN GREECE - USE OF COAGULATION FACTOR-IX GENE PROBES FOR CARRIER DETECTION RICERCA IN CLINICA E IN LABORATORIO, 1986, 16 (01): : 155 - 156
- [6] CARRIER DETECTION BY DIRECT GENE ANALYSIS IN A FAMILY WITH HEMOPHILIA-B (FACTOR-IX DEFICIENCY) LANCET, 1984, 1 (8371): : 242 - 243
- [7] A NEW POLYMORPHISM IN A HUMAN FACTOR-IX GENE USEFUL FOR DETECTION OF HEMOPHILIA-B CARRIERS GENETIKA, 1994, 30 (06): : 740 - 742
- [9] AN INTRAGENIC DELETION OF THE FACTOR-IX GENE IN A FAMILY WITH HEMOPHILIA-B JOURNAL OF CLINICAL INVESTIGATION, 1985, 76 (06): : 2161 - 2164