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Factor VII and factor X deficiency in a child with a chromosome 13q duplication and deletion

  • Published:2017-06-04 Issue:1 Volume:27 Page:
  • ISSN:1351-8216
  • Container-title:Haemophilia
  • language:en
  • Short-container-title:Haemophilia

Author:

Hutchins K.12,Rajpurkar M.12,Stockton D. W.23,Callaghan M. U.12

Affiliation:

1. Carmen and Ann Adams Department of Pediatrics Division of Hematology/Oncology Children's Hospital of MichiganDetroit MI USA

2. Department of Pediatrics Wayne State UniversityDetroit MI USA

3. Carmen and Ann Adams Department of Pediatrics Division of Genetic, Genomic and Metabolic Disorders Children's Hospital of Michigan Detroit MI USA

Publisher

Wiley

Subject

Genetics (clinical),Hematology,General Medicine

Reference9 articles.

1. 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)

2. Evidence that Activities of Coagulation Factors VII and X are Linked to Chromosome 13 (q34)

3. The structural gene for human coagulation factor X is located on chromosome 13q34

4. [De novo del (13) (q31.1—qter) in a girl. Effect of gene dosage on blood coagulation factors VII and X];Battin J;J Genet Hum,1988

5. Two cases of terminal deletion of chromosome 13: clinical features, conventional and molecular cytogenetic analysis;Luquet I;Ann Genet,1999

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