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Items: 1 to 20 of 121

1.

A transcribed gene in an intron of the human factor VIII gene.

Levinson B, Kenwrick S, Lakich D, Hammonds G Jr, Gitschier J.

Genomics. 1990 May;7(1):1-11.

PMID:
2110545
2.

Evidence for a third transcript from the human factor VIII gene.

Levinson B, Kenwrick S, Gamel P, Fisher K, Gitschier J.

Genomics. 1992 Nov;14(3):585-9.

PMID:
1427887
3.

Isolation and sequence of two genes associated with a CpG island 5' of the factor VIII gene.

Kenwrick S, Levinson B, Taylor S, Shapiro A, Gitschier J.

Hum Mol Genet. 1992 Jun;1(3):179-86.

PMID:
1303175
4.
6.
7.

Analysis of large structural changes of the factor VIII gene, involving intron 1 and 22, in severe hemophilia A.

Andrikovics H, Klein I, Bors A, Nemes L, Marosi A, Váradi A, Tordai A.

Haematologica. 2003 Jul;88(7):778-84.

8.

Nucleotide sequence of the gene for the b subunit of human factor XIII.

Bottenus RE, Ichinose A, Davie EW.

Biochemistry. 1990 Dec 25;29(51):11195-209.

PMID:
2271707
9.

Variation of the non-factor VIII sequences detected by a probe from intron 22 of the factor VIII gene.

Lillicrap DP, Taylor SA, Schuringa PC, Blanchette VS, Lovsted JK, Weiler LJ, Bridge PJ.

Blood. 1990 Jan 1;75(1):139-43.

10.

Recurrent inversion breaking intron 1 of the factor VIII gene is a frequent cause of severe hemophilia A.

Bagnall RD, Waseem N, Green PM, Giannelli F.

Blood. 2002 Jan 1;99(1):168-74.

11.

Factor VIII gene inversions in severe hemophilia A patients.

Van de Water NS, Williams R, Nelson J, Browett PJ.

Pathology. 1995 Jan;27(1):83-5.

PMID:
7603762
12.

Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A.

Lakich D, Kazazian HH Jr, Antonarakis SE, Gitschier J.

Nat Genet. 1993 Nov;5(3):236-41.

PMID:
8275087
14.

Factor VIII gene deletions in haemophilia A patients in Czechoslovakia.

Krepelová A, Vorlová Z, Zavadil J, Brdicka R.

Br J Haematol. 1992 Jun;81(2):271-6.

PMID:
1643024
16.

Investigation of the factor VIII intron 22 repeated region (int22h) and the associated inversion junctions.

Naylor JA, Buck D, Green P, Williamson H, Bentley D, Giannelli F.

Hum Mol Genet. 1995 Jul;4(7):1217-24.

PMID:
8528212
18.

Nonhomologous recombination in the human genome: deletions in the human factor VIII gene.

Woods-Samuels P, Kazazian HH Jr, Antonarakis SE.

Genomics. 1991 May;10(1):94-101.

PMID:
1904396
19.

CpG islands of the X chromosome are gene associated.

Alcalay M, Toniolo D.

Nucleic Acids Res. 1988 Oct 25;16(20):9527-43.

20.

Characteristic mRNA abnormality found in half the patients with severe haemophilia A is due to large DNA inversions.

Naylor J, Brinke A, Hassock S, Green PM, Giannelli F.

Hum Mol Genet. 1993 Nov;2(11):1773-8.

PMID:
8281136
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