114 related articles for article (PubMed ID: 15754755)
21. [Molecular diagnosis in patients and carriers of hemophilia A and B].
Mantilla-Capacho J; Beltrán-Miranda CP; Jaloma-Cruz AR
Gac Med Mex; 2005; 141(1):69-71. PubMed ID: 15754755
[No Abstract] [Full Text] [Related]
22. [Structure and function of factor VIII and factor IX gene and molecular DNA diagnosis in hemophilia A and B].
Herrmann FH; Wehnert M; Wulff K
Z Arztl Fortbild (Jena); 1988; 82(22):1116-22. PubMed ID: 2907834
[No Abstract] [Full Text] [Related]
23. Molecular basis of hemophilia.
Lozier JN; High KA
Hematol Pathol; 1990; 4(1):1-26. PubMed ID: 2111315
[No Abstract] [Full Text] [Related]
24. [Gene mutation and gene diagnosis of hemophilia].
Kojima T
Nihon Seirigaku Zasshi; 1998; 60(1):31-42. PubMed ID: 9614303
[No Abstract] [Full Text] [Related]
25. Molecular biology of the hemophilias.
Thompson AR
Prog Hemost Thromb; 1991; 10():175-214. PubMed ID: 1901173
[No Abstract] [Full Text] [Related]
26. The molecular genetics of haemophilia A and B.
Brownlee GG
J Cell Sci Suppl; 1986; 4():445-58. PubMed ID: 3091610
[No Abstract] [Full Text] [Related]
27. Hemophilia A and B: molecular and clinical similarities and differences.
Castaman G; Matino D
Haematologica; 2019 Sep; 104(9):1702-1709. PubMed ID: 31399527
[No Abstract] [Full Text] [Related]
28. Recent advances in the management of the child who has hemophilia.
Dunn AL; Abshire TC
Hematol Oncol Clin North Am; 2004 Dec; 18(6):1249-76, viii. PubMed ID: 15511615
[TBL] [Abstract][Full Text] [Related]
29. Status of gene transfer for hemophilia A and B.
Thompson AR
Thromb Haemost; 1991 Jul; 66(1):119-22. PubMed ID: 1926041
[No Abstract] [Full Text] [Related]
30. From hemophilia B to hemophilia A via the fragile X locus: genes and recombination in the distal region of the human X chromosome long arm.
Oberlé I; Mandel JL
Horiz Biochem Biophys; 1986; 8():51-89. PubMed ID: 2875934
[No Abstract] [Full Text] [Related]
31. The molecular genetics of hemophilia A and B in man. Factor VIII and factor IX deficiency.
Antonarakis SE
Adv Hum Genet; 1988; 17():27-59. PubMed ID: 3142226
[No Abstract] [Full Text] [Related]
32. Factor IX molecular defects in diagnosing hemophilia B: a review.
Tanimoto M
Nihon Ketsueki Gakkai Zasshi; 1989 Jul; 52(4):811-5. PubMed ID: 2694721
[TBL] [Abstract][Full Text] [Related]
33. [Hemophilia].
Shima M
Rinsho Ketsueki; 2013 Feb; 54(2):189-97. PubMed ID: 23470826
[No Abstract] [Full Text] [Related]
34. Detection of carriers and prenatal diagnosis of bleeding disorders.
Peake I
Southeast Asian J Trop Med Public Health; 1993; 24 Suppl 1():37-40. PubMed ID: 7886602
[TBL] [Abstract][Full Text] [Related]
35. Hereditary disorders of blood coagulation.
Zieve PD; Levin J
Major Probl Intern Med; 1976; 10():51-64. PubMed ID: 785116
[No Abstract] [Full Text] [Related]
36. Haemophilia: strategies for carrier detection and prenatal diagnosis.
Peake IR; Lillicrap DP; Boulyjenkov V; Briet E; Chan V; Ginter EK; Kraus EM; Ljung R; Mannucci PM; Nicolaides K
Bull World Health Organ; 1993; 71(3-4):429-58. PubMed ID: 8324863
[TBL] [Abstract][Full Text] [Related]
37. Molecular biology of coagulation.
Pavirani A; Bischoff R
Schweiz Med Wochenschr Suppl; 1991; 43():55-7. PubMed ID: 1843038
[No Abstract] [Full Text] [Related]
38. [Gene therapy for hemophilia].
Mimuro J; Sakata Y
Nihon Rinsho; 2005 Dec; 63 Suppl 12():646-54. PubMed ID: 16416868
[No Abstract] [Full Text] [Related]
39. Challenges of multiple mutations in individual patients with haemophilia.
Shetty S; Bhave M; Ghosh K
Eur J Haematol; 2011 Mar; 86(3):185-90. PubMed ID: 21175850
[TBL] [Abstract][Full Text] [Related]
40. Biology of inherited coagulopathies: factor IX.
Larson PJ; High KA
Hematol Oncol Clin North Am; 1992 Oct; 6(5):999-1009. PubMed ID: 1356960
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]