Lillicrap DP, et al. Variation of the non-factor VIII sequences detected by a probe from intron 22 of the factor VIII gene. Blood 75: 139-143, 1990. PubMed: 1967212
Taylor SA, et al. A BstXI polymorphism detected by the factor VIII genomic probe p482.6 (F8C). Nucleic Acids Res. 17: 6426, 1989. PubMed: 2570405
Suthers GK, et al. Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines. Am. J. Hum. Genet. 47: 187-195, 1990. PubMed: 2378346
Janco RL, et al. Improved efficacy of carrier assignment in hemophilia A using intragenic probes. Am. J. Hum. Genet. 39: A95, 1986.
Youssoufian H, et al. Characterization of five partial deletions of the factor VIII gene. Proc. Natl. Acad. Sci. USA 84: 3772-3776, 1987. PubMed: 3035554
Wion KL, et al. A new polymorphism in the factor VIII gene for prenatal diagnosis of hemophilia A. Nucleic Acids Res. 14: 4535-4542, 1986. PubMed: 3012474
|
