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2. Genetic counseling in classic hemophilia A. Graham JB N Engl J Med; 1977 Apr; 296(17):996-8. PubMed ID: 846546 [No Abstract] [Full Text] [Related]
3. Detection of the carrier state for classic hemophilia. Bennett B; Ratnoff OD N Engl J Med; 1973 Feb; 288(7):342-5. PubMed ID: 4682943 [No Abstract] [Full Text] [Related]
5. Proceedings: Detection of carriers of haemophilia using linear discriminant analysis. Prentice CR; Forbes CD; Smith S; McLaren D Br J Haematol; 1974 Jun; 27(2):364-5. PubMed ID: 4846284 [No Abstract] [Full Text] [Related]
6. [Detection of Hemophilia A carrier state]. Michalski R; Pniejnia-Olszyński W; Bykowska K; Lopaciuk S Acta Haematol Pol; 1977; 8(3):229-33. PubMed ID: 920063 [TBL] [Abstract][Full Text] [Related]
7. [Method of detecting the transmission of hemophilia: report of the WHO]. Bull World Health Organ; 1979; 57(4):579-609. PubMed ID: 316737 [No Abstract] [Full Text] [Related]
9. Hemophilia A carrier detection by restriction fragment length polymorphism analysis and discriminant analysis based on ELISA of factor VIII and vWf. Poon MC; Hoar DI; Low S; Pon JK; Anand S; Sinclair GD J Lab Clin Med; 1992 Jun; 119(6):751-62. PubMed ID: 1350611 [TBL] [Abstract][Full Text] [Related]
10. Carrier analysis for hemophilia A: ideal versus acceptable. Husain N Expert Rev Mol Diagn; 2009 Apr; 9(3):203-7. PubMed ID: 19379077 [No Abstract] [Full Text] [Related]
11. Inversion of intron 22 in isolated cases of severe hemophilia A. Tizzano EF; Domènech M; Baiget M Thromb Haemost; 1995 Jan; 73(1):6-9. PubMed ID: 7740498 [TBL] [Abstract][Full Text] [Related]
12. Clinical correlates among 49 families with hemophilia A and factor VIII gene inversions. Weinmann AF; Schoof JM; Thompson AR Am J Hematol; 1996 Mar; 51(3):192-9. PubMed ID: 8619399 [TBL] [Abstract][Full Text] [Related]
13. [Molecular biologic study and the factor VIII gene in hemophilia A]. Bock I; Melegh B; Nagy A; Losonczy H; Csete B; Schröder W; Kardos M; István L; Jager R; Tóth AM; Tóth A; Falko H; Mózsik G Orv Hetil; 1996 Nov; 137(46):2573-5. PubMed ID: 9005386 [TBL] [Abstract][Full Text] [Related]
14. [Carrier detection and prenatal diagnosis for hemophilia A using the inversion analysis of the factor VIII gene]. Okamoto Y; Kojima T; Katsumi A; Yamazaki T; Hamaguchi M; Nishida M; Suzumori K; Saito H Rinsho Ketsueki; 1995 Nov; 36(11):1252-6. PubMed ID: 8691564 [TBL] [Abstract][Full Text] [Related]
15. Molecular genetics and counselling in haemophilia. Peake I Thromb Haemost; 1995 Jul; 74(1):40-4. PubMed ID: 8578494 [TBL] [Abstract][Full Text] [Related]
16. [The genetic questionnaire. Genetic advice given to a family affected by hemophilia A (Factor VIII deficiency)]. Pfändler U J Genet Hum; 1968 Jan; 16(3):103-5. PubMed ID: 5710708 [No Abstract] [Full Text] [Related]
17. [Current possibilities in the laboratory detection of hemophilia A carrier state]. Procházka J; Blatný J; Fischerová E; Smrcková H; Manáková D Vnitr Lek; 1978 Jan; 24(1):32-9. PubMed ID: 625894 [No Abstract] [Full Text] [Related]
18. [Gene diagnosis of hemophilia A]. Shen Y Zhonghua Yi Xue Za Zhi; 1989 Aug; 69(8):422-6, 30. PubMed ID: 2575928 [TBL] [Abstract][Full Text] [Related]
19. [Principles of medical genetic consultation in hemophilia A]. Pliush OP; Snegireva-Davydenko IB; Khametova RN; Likhacheva EA; Brodskaia TV Gematol Transfuziol; 1986 Nov; 31(11):21-5. PubMed ID: 3100381 [No Abstract] [Full Text] [Related]
20. Concurrence of von Willebrand's disease and hemophilia A: implications for carrier detection and prevalence. Miller CH; Hilgartner MW; Harris MB; Bussel JB; Aledort LM Am J Med Genet; 1986 May; 24(1):83-94. PubMed ID: 3085499 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]