Reply to the letter by Kling et al.
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00215690.pdf
Reference8 articles.
1. Chan V, Tong TMF, Chan TPT, Tang M, Wan CW, Chan FY, Chu YC, Chan TK (1990) Multiple XbaI polymorphisms for carrier detection and prenatal diagnosis of hemophilia A. Br J Haematol 73:497–500
2. Kling S, Ljung R, Sjörin E, Nilsson IM (1992) Further characterization of the new marker at DXS115 with regard to carrier detection in hemophilia A. Hum Genet 88:484
3. Kogan SC, Doherty M, Gitschier J (1987) An improved method for prental diagnosis of genetic diseases by analysis of amplified DNA sequences. N Engl J Med 317:985–990
4. Levinson B, Kenwrick S, Lakich D, Hammonds G, Gitschier J (1990) A transcribed gene in an intron of the human factor VIII gene. Genomics 7: 1–11
5. Lillicrap DP, Taylor SAM, Schuringa PCR, Blanchette VS, Lovsted JK, Weiler LJ, Brigde PJ (1990) Variation of the non-factor VIII sequences detected by a probe from intron 22 of the factor VIII gene. Blood 75:139–143
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