Deletion of the factor IX gene as a result of translocation t(X;1) in a girl affected by haemophilia B-Reference-Cited by-同舟云学术

Deletion of the factor IX gene as a result of translocation t(X;1) in a girl affected by haemophilia B

Published:2001-06 Issue:3 Volume:113 Page:616-620
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:

Author:

Krepischi-Santos A. C. V.,Carneiro J. D. A.,Svartman M.,Bendit I.,Odone-Filho V.,Vianna-Morgante A. M.

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.2001.02786.x/fullpdf

Reference17 articles.

1. Molecular analysis of a constitutional X-Autosome translocation in a female with muscular dystrophy;Bodrug;Science,1987

2. X chromosome inactivation and the diagnosis of X linked disease in females;Brown;Journal of Medical Genetics,1993

3. Isolation and characterization of a human variable copy number tandem repeat at Xcen-p11.22;Fraser;Genomics,1989

4. Common sequence motifs at the rearrangements sites of a constitutional X/Autosome translocation and associated deletion;Giacalone;American Journal of Human Genetics,1992

5. Moderate haemophilia B in a female carrier caused by preferential inactivation of the paternal X chromosome;Kling;European Journal of Haematology,1991

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