Activity and antigen of coagulation factors VII and X in five patients with abnormal chromosome 13

Author:

Fukushima Yoshimitsu,Kuroki Yoshikazu,Iizuka Atsushi

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical)

Reference6 articles.

1. Cox, D.R. and Gedde-Dahl, Jr., T. 1985. Report of the committee on the genetic constitution of chromosomes 13, 14, 15 and 16.Cytogenet. Cell Genet. 40 (1–4), Human Gene Mapping 8: 206–241.

2. de Grouchy, J., Dautzenberg, M.-D., Turleau C., Beguin, S., and Chavin-Colin, F. 1984. Regional mapping of clotting factors VII and X to 13q34. Expression of factor VII through chromosome 8.Hum. Genet. 66:230–233.

3. Kajii, T., Tsukahara, M., Fukushima, Y., Hata, A., Matsuo, K., and Kuroki, Y. 1985. Translocation (X;13)(p11.21;q12.3) in a girl with incontinentia pigmenti and bilateral retinoblastoma.Ann. Génét. 28:219–223.

4. Niebuhr, E. 1977. Partial trisomies and deletions of chromosome 13. InNew Chromosomal Syndromes, Yunis, J.J. ed., Academic Press, New York, pp. 273–299.

5. Ott, R. and Pfeiffer, R.A. 1984. Evidence that activities of coagulation factors VII and X are linked to chromosome 13(q34).Hum. Hered. 34:123–126.

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