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410 related items for PubMed ID: 18702107
21. Implications of gene sequencing in the direct diagnosis of hemophilia by PCR-RFLP. Vidal F, Farssac E, Altisent C, Puig L, Gallardo D. Haematologica; 2002 Jan; 87(1):109-10. PubMed ID: 11801473 [No Abstract] [Full Text] [Related]
22. Molecular genetics of hemophilia A. Gitschier J. Schweiz Med Wochenschr; 1989 Sep 30; 119(39):1329-31. PubMed ID: 2508218 [Abstract] [Full Text] [Related]
23. Carrier detection in hemophilia using pedigree analysis coagulation tests and DNA probes. de la Salle C, Baas MJ, Grunebaum L, Wiesel ML, Blanco A, Gialeraki R, Mandalaki T, Cazenave JP. Nouv Rev Fr Hematol (1978); 1989 Sep 30; 31(3):193-202. PubMed ID: 2575737 [Abstract] [Full Text] [Related]
24. [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 30; 36(11):1252-6. PubMed ID: 8691564 [Abstract] [Full Text] [Related]
29. Allele frequencies of two polymorphisms associated with the factor IX gene in Iranian population. Ghandil P, Ghadiri A, Farhud D, Zeinali S. Thromb Res; 2004 Nov 30; 113(5):289-93. PubMed ID: 15183040 [Abstract] [Full Text] [Related]
31. Polymorphism distribution of Int13, Int22, and St14 VNTRs in a Mexican population and their application in carrier diagnosis of hemophilia A. Gallegos RM, Aranda HB, Navarrete CP, Espinoza R, Gómez FS, Aranda DA. Am J Hematol; 2004 Sep 30; 77(1):1-6. PubMed ID: 15307098 [Abstract] [Full Text] [Related]
33. Identification of missense mutations in exon 16 of factor VIII gene in mild and moderate cases with hemophilia A. Faridi NJ, Husain N, Siddiqi MI, Kumar P, Bamezai RN. Clin Appl Thromb Hemost; 2011 Aug 30; 17(4):358-61. PubMed ID: 20460344 [Abstract] [Full Text] [Related]
38. [Gene mutation and gene diagnosis of hemophilia]. Kojima T. Nihon Seirigaku Zasshi; 1998 Aug 30; 60(1):31-42. PubMed ID: 9614303 [No Abstract] [Full Text] [Related]
40. Mutational-screening in the factor VIII gene resulting in the identification of three novel mutations, one of which is a donor splice mutation. Mutations in brief no. 245. Online. Möller-Morlang K, Tavassoli K, Eigel A, Pollmann H, Horst J. Hum Mutat; 1999 Aug 30; 13(6):504. PubMed ID: 10408784 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]