130 related articles for article (PubMed ID: 367659)
1. Genotype assignment (carrier detection) in the haemophilias.
Graham JB
Clin Haematol; 1979 Feb; 8(1):115-45. PubMed ID: 367659
[No Abstract] [Full Text] [Related]
2. Recent advances in the detection of carriers of haemophilia A, B and Von Willebrand's disease.
Schinco PM; Rizza CR
Haematologica; 1983; 68(1):124-34. PubMed ID: 6404703
[No Abstract] [Full Text] [Related]
3. [Genetic aspects of hemophilia A and B].
Veltkamp JJ
Ned Tijdschr Geneeskd; 1975 Jan; 119(1):17-22. PubMed ID: 1088978
[No Abstract] [Full Text] [Related]
4. 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]
5. [Contribution of genetic analysis in management of hemophilie patients].
Vinciguerra C; Frétigny M; Négrier C
Arch Pediatr; 2010 Jun; 17(6):620-1. PubMed ID: 20654809
[No Abstract] [Full Text] [Related]
6. 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]
7. [Carrier state of hemophilia].
Mauser-Bunschoten EP; Veltkamp JJ; van Leeuwen EF; Sjamsoedin-Visser EJ
Ned Tijdschr Geneeskd; 1984 Feb; 128(8):350-4. PubMed ID: 6700779
[No Abstract] [Full Text] [Related]
8. [Hemophilia, carrier state and prenatal diagnosis].
Sixma JJ
Ned Tijdschr Geneeskd; 1984 Feb; 128(8):360-2. PubMed ID: 6700781
[No Abstract] [Full Text] [Related]
9. [Proceedings: Genetic aspects of hereditary coagulopathies].
Rasore-Quartino A
Minerva Pediatr; 1973 Nov; 25(41):1846-67. PubMed ID: 4544077
[No Abstract] [Full Text] [Related]
10. Haemophilia carrier detection using DNA analysis.
Van-de-Water NS; Ockelford PA
N Z Med J; 1988 Sep; 101(853):584. PubMed ID: 2901705
[No Abstract] [Full Text] [Related]
11. Genetic counseling of hemophilia carriers.
Ljung R; Tedgård U
Semin Thromb Hemost; 2003 Feb; 29(1):31-6. PubMed ID: 12640562
[TBL] [Abstract][Full Text] [Related]
12. [Hereditary disorders of blood coagulation with hemorrhagic diathesis].
Schramm W
Internist (Berl); 1989 Sep; 30(9):567-76. PubMed ID: 2681041
[No Abstract] [Full Text] [Related]
13. Methods for the detection of haemophilia carriers: a memorandum.
Bull World Health Organ; 1977; 55(6):675-702. PubMed ID: 304395
[TBL] [Abstract][Full Text] [Related]
14. [Molecular biology of blood coagulation disorders].
Saito H
Nihon Naika Gakkai Zasshi; 1991 Oct; 80(10):1682-6. PubMed ID: 1685509
[No Abstract] [Full Text] [Related]
15. Comparison of direct and indirect methods of carrier detection in an X-linked disease.
Koeberl DD; Bottema CD; Sommer SS
Am J Med Genet; 1990 Apr; 35(4):600-8. PubMed ID: 1970704
[No Abstract] [Full Text] [Related]
16. Genetic analysis of von Willebrand's disease in two large pedigrees: a multivariate approach.
Goldin LR; Elston RC; Graham JB; Miller CH
Am J Med Genet; 1980; 6(4):279-93. PubMed ID: 6782878
[TBL] [Abstract][Full Text] [Related]
17. Haemophilia management: the application of DNA analysis for prenatal diagnosis.
Van de Water NS; Ockelford PA; Berry EW; Browett PJ
N Z Med J; 1991 Oct; 104(922):443-6. PubMed ID: 1681487
[TBL] [Abstract][Full Text] [Related]
18. [Occurrence of hemophilia A and von Willebrand disease in the same family].
Shinmyozu K; Okadome T; Maruyama Y; Maruyama I; Osame M
Rinsho Ketsueki; 1990 May; 31(5):665-8. PubMed ID: 2395214
[TBL] [Abstract][Full Text] [Related]
19. [Diagnosis of hemophilia A and B by recombinant DNA methods].
Lehesjoki AE; Rasi V; de la Chapelle A
Duodecim; 1987; 103(14):867-75. PubMed ID: 2895703
[No Abstract] [Full Text] [Related]
20. Hereditary and acquired hemorrhagic disorders in animals.
Dodds WJ
Prog Hemost Thromb; 1974; 2(0):215-47. PubMed ID: 4604529
[No Abstract] [Full Text] [Related]
[Next] [New Search]