Molecular characterization of a 4 409 480 bp deletion of the human X chromosome in a patient with haemophilia B-Reference-Cited by-同舟云学术

Molecular characterization of a 4 409 480 bp deletion of the human X chromosome in a patient with haemophilia B

Author:

Hewitt J.¹²,Chou E. M. H.¹²,Brown L. A.³⁴,Smith V. C.¹²,Yong S.-L.⁵⁶,Wadsworth L. D.²⁴⁶,Wu J. K.²⁶⁷,MacGillivray R. T. A.¹²

Affiliation:

1. Department of Biochemistry & Molecular Biology; University of British Columbia; Vancouver BC Canada

2. Centre for Blood Research; University of British Columbia; Vancouver BC Canada

3. Genetic Pathology Evaluation Centre of the Prostate Centre; BC Cancer Agency; Vancouver BC Canada

4. Department of Pathology & Laboratory Medicine; University of British Columbia; Vancouver BC Canada

5. Department of Medical Genetics; University of British Columbia; Vancouver BC Canada

6. B.C. Children's & Women's Health Centre; Vancouver BC Canada

7. Department of Pediatrics; University of British Columbia; Vancouver BC Canada

Publisher

Wiley

Subject

Genetics(clinical),Hematology,General Medicine

Link

Reference10 articles.

3. The rates and patterns of deletions in the human factor IX gene;Ketterling;Am J Hum Genet,1994

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