Cited by

• The contribution of DNA analysis to carrier detection and prenatal diagnosis of hemophilia A and B.

  Bröcker-Vriends AH, Bakker E, Kanhai HH, van Ommen GJ, Reitsma PH, van de Kamp JJ, Briët E. Bröcker-Vriends AH, et al. Ann Hematol. 1992 Jan;64(1):2-11. doi: 10.1007/BF01811464. Ann Hematol. 1992. PMID: 1739755 Review.
• RFLP analysis in families with sporadic hemophilia A. Estimate of the mutation ratio in male and female gametes.

  Bernardi F, Marchetti G, Bertagnolo V, Faggioli L, Volinia S, Patracchini P, Bartolai S, Vannini F, Felloni L, Rossi L, et al. Bernardi F, et al. Hum Genet. 1987 Jul;76(3):253-6. doi: 10.1007/BF00283618. Hum Genet. 1987. PMID: 2885255
• De novo mutation in hemophilia A established by DNA haplotype analysis and precluding prenatal diagnosis.

  Delpech M, Deburgrave N, Baudis M, Maissonneuve P, Bardin JM, Sultan Y, Kaplan JC. Delpech M, et al. Hum Genet. 1986 Nov;74(3):316-7. doi: 10.1007/BF00282556. Hum Genet. 1986. PMID: 2877941
• Sex ratio of the mutation frequencies in haemophilia A: coagulation assays and RFLP analysis.

  Bröcker-Vriends AH, Rosendaal FR, van Houwelingen JC, Bakker E, van Ommen GJ, van de Kamp JJ, Briët E. Bröcker-Vriends AH, et al. J Med Genet. 1991 Oct;28(10):672-80. doi: 10.1136/jmg.28.10.672. J Med Genet. 1991. PMID: 1682494 Free PMC article.
• A new polymorphism in the factor VIII gene for prenatal diagnosis of hemophilia A.

  Wion KL, Tuddenham EG, Lawn RM. Wion KL, et al. Nucleic Acids Res. 1986 Jun 11;14(11):4535-42. doi: 10.1093/nar/14.11.4535. Nucleic Acids Res. 1986. PMID: 3012474 Free PMC article.