Severe congenital Factor VII deficiency associated with the 13q deletion syndrome
Open Access
- 30 October 2002
- journal article
- case report
- Published by Wiley in American Journal of Hematology
- Vol. 71 (3) , 232-233
- https://doi.org/10.1002/ajh.10237
Abstract
The first reported case of clinically significant congenital Factor VII deficiency in association with the 13q deletion syndrome is presented. It illustrates the importance of knowledge of the specific genes involved in gross deletion syndromes and adds to the current clinical experience of this rare disease. Am. J. Hematol. 71:232–233, 2002.Keywords
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- Deficiency of coagulation factors VII and X associated with deletion of a chromosome 13 (q34). Evidence from two cases with 46,XY,t(13;Y)(q11;q34)Human Genetics, 1982