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Results: 1-12 |
Results: 12

Authors: PEYVANDI F MANNUCCI PM JENKINS PV PERRY DJ
Citation: F. Peyvandi et al., DETECTION OF THE MOLECULAR LESIONS IN 29 FAMILIES WITH FACTOR-VII DEFICIENCY, Thrombosis research, 91(3), 1998, pp. 6-6

Authors: JENKINS PV ONONYE C PASI KJ
Citation: Pv. Jenkins et al., IDENTIFICATION OF A NOVEL CANDIDATE MUTATION CAUSING 2A (IID) VON-WILLEBRANDS-DISEASE, Thrombosis research, 91(3), 1998, pp. 28-28

Authors: JENKINS PV PASI KJ PERKINS SJ
Citation: Pv. Jenkins et al., MOLECULAR MODELING OF LIGAND AND MUTATION SITES OF THE A1 AND A2 DOMAINS OF HUMAN VON-WILLEBRAND-FACTOR AND THEIR RELEVANCE TO VON-WILLEBRANDS-DISEASE, British Journal of Haematology, 101, 1998, pp. 251-251

Authors: JENKINS PV PASI KJ PERKINS SJ
Citation: Pv. Jenkins et al., MOLECULAR MODELING OF LIGAND AND MUTATION SITES OF THE TYPE-A DOMAINSOF HUMAN VON-WILLEBRAND-FACTOR AND THEIR RELEVANCE TO VON-WILLEBRANDS-DISEASE, Blood, 91(6), 1998, pp. 2032-2044

Authors: JENKINS PV PASI KJ ONONYE C PERKINS SJ
Citation: Pv. Jenkins et al., A MOLECULAR GRAPHICS MODEL OF THE A1 AND A2 DOMAINS OF VON-WILLEBRAND-FACTOR, Thrombosis and haemostasis, 1997, pp. 1493-1493

Authors: PASI KJ ONONYE C JENKINS PV SABIN CA LEE CA
Citation: Kj. Pasi et al., ANALYSIS OF CKR5 MUTANTS IN HIV-INFECTED HEMOPHILIC PATIENTS AND HIV EXPOSED BUT UNINFECTED HEMOPHILIC PATIENTS, Blood, 88(10), 1996, pp. 2604-2604

Authors: ONONYE C JENKINS PV GOLDMAN E PASI KJ
Citation: C. Ononye et al., CARRIER DETECTION AND PRENATAL-DIAGNOSIS BY INTRON-22 INVERSION ANALYSIS OF THE FACTOR-VIII GENE, Haemophilia, 1(3), 1995, pp. 204-206

Authors: ANTONARAKIS SE ROSSITER JP YOUNG M HORST J DEMOERLOOSE P SOMMER SS KETTERLING RP KAZAZIAN HH NEGRIER C VINCIGUERRA C GITSCHIER J GOOSSENS M GIRODON E GHANEM N PLASSA F LAVERGNE JM VIDAUD M COSTA JM LAURIAN Y LIN SW LIN SR SHEN MC LILLICRAP D TAYLOR SAM WINDSOR S VALLEIX SV NAFA K SULTAN Y DELPECH M VNENCAKJONES CL PHILLIPS JA LJUNG RCR KOUMBARELIS E GIALERAKI A MANDALAKI T JENKINS PV COLLINS PW PASI KJ GOODEVE A PEAKE I PRESTON FE SCHWARTZ M SCHEIBEL E INGERSLEV J COOPER DN MILLAR DS KAKKAR VV GIANNELLI F NAYLOR JA TIZZANO EF BAIGET M DOMENECH M ALTISENT C TUSELL J BENEYTO M LORENZO JI GAUCHER C MAZURIER C PEERLINCK K MATTHIJS G CASSIMAN JJ VERMYLEN J MORI PG ACQUILA M CAPRINO D INABA H
Citation: Se. Antonarakis et al., FACTOR-VIII GENE INVERSIONS IN SEVERE HEMOPHILIA-A - RESULTS OF AN INTERNATIONAL CONSORTIUM STUDY, Blood, 86(6), 1995, pp. 2206-2212

Authors: JENKINS PV ONONYE C COLLINS PW PASI KJ
Citation: Pv. Jenkins et al., DOMINANT TYPE-1 VONWILLEBRANDS-DISEASE AS A RESULT OF A 4 BASE-PAIR DELETION IN EXON-28 OF THE VON-WILLEBRAND-FACTOR GENE, Blood, 86(10), 1995, pp. 265-265

Authors: COLLINS PW JENKINS PV GOLDMAN E LEE CA PASI KJ
Citation: Pw. Collins et al., INTRON-22 INVERSIONS AND HEMOPHILIA, Lancet, 343(8900), 1994, pp. 791-791

Authors: JENKINS PV COLLINS PW GOLDMAN E MCCRAW A RIDDELL A LEE CA PASI KJ
Citation: Pv. Jenkins et al., ANALYSIS OF INTRON-22 INVERSIONS OF THE FACTOR-VIII GENE IN SEVERE HEMOPHILIA-A - IMPLICATIONS FOR GENETIC-COUNSELING, Blood, 84(7), 1994, pp. 2197-2201

Authors: PASI KJ ENAYAT MS JENKINS PV LEE CA HILL FGH
Citation: Kj. Pasi et al., FAMILY STUDIES IN VON-WILLEBRANDS DISEASE USING VARIABLE NUMBER TANDEM REPEATS AND RESTRICTION POLYMORPHISM ANALYSIS OF THE VON-WILLEBRAND-FACTOR GENE, Thrombosis and haemostasis, 69(6), 1993, pp. 1179-1179
Risultati: 1-12 |