Skip to main content
NCBI home page
American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 1973 Jan;25(1):57–61.

Retinoblastoma and D-chromosome deletions.

M G Wilson, J W Towner, A Fujimoto
PMCID: PMC1762223  PMID: 4119334

Full text

PDF
57

Images in this article

58Fig. 1
on p.58
59Fig. 2
on p.59

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Allderdice P. W., Davis J. G., Miller O. J., Klinger H. P., Warburton D., Miller D. A., Allen F. H., Jr, Abrams C. A., McGilvray E. The 13q-deletion syndrome. Am J Hum Genet. 1969 Sep;21(5):499–512. [PMC free article] [PubMed] [Google Scholar]
  2. Coffin G. S., Wilson M. G. Ring chromosome D (13). Am J Dis Child. 1970 Apr;119(4):370–373. doi: 10.1001/archpedi.1970.02100050372020. [DOI] [PubMed] [Google Scholar]
  3. De Capoa A., Miller D. A., Miller O. J. Asynchronous DNA replication and discordant length of homologous autosomes demonstrated by the use of markers. Nature. 1968 Oct 19;220(5164):264–266. doi: 10.1038/220264a0. [DOI] [PubMed] [Google Scholar]
  4. Drets M. E., Shaw M. W. Specific banding patterns of human chromosomes. Proc Natl Acad Sci U S A. 1971 Sep;68(9):2073–2077. doi: 10.1073/pnas.68.9.2073. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Gey W. Dq-, multiple Missbildungen und Retinoblastom. Humangenetik. 1970;10(4):362–365. doi: 10.1007/BF00278776. [DOI] [PubMed] [Google Scholar]
  6. Grace E., Drennan J., Colver D., Gordon R. R. The 13q- deletion syndrome. J Med Genet. 1971 Sep;8(3):351–357. doi: 10.1136/jmg.8.3.351. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. LELE K. P., PENROSE L. S., STALLARD H. B. CHROMOSOME DELETION IN A CASE OF RETINOBLASTOMA. Ann Hum Genet. 1963 Nov;27:171–174. doi: 10.1111/j.1469-1809.1963.tb00209.x. [DOI] [PubMed] [Google Scholar]
  8. Lehrke R., Thelen T., Lehrke R., Jr Syndrome associated with group-D chromosome deletions. Lancet. 1971 Jul 10;2(7715):98–99. doi: 10.1016/s0140-6736(71)92075-7. [DOI] [PubMed] [Google Scholar]
  9. Miller O. J., Breg W. R., Warburton D., Miller D. A., Firschein I. L., Hirschhorn K. Alternative DNA replication patterns associated with long arm length of chromosomes 4 and 5 in the cri du chat syndrome. Cytogenetics. 1966;5(3):137–151. doi: 10.1159/000129893. [DOI] [PubMed] [Google Scholar]
  10. Orbeli D. J., Lurie I. W., Goroshenko J. L. The syndrome associated with the partial D-monosomy. Case report and review. Humangenetik. 1971;13(4):296–308. doi: 10.1007/BF00273945. [DOI] [PubMed] [Google Scholar]
  11. Orye E., Delbeke M. J., Vandenabeele B. Retinoblastoma and D-chromosome deletions. Lancet. 1971 Dec 18;2(7738):1376–1376. doi: 10.1016/s0140-6736(71)92394-4. [DOI] [PubMed] [Google Scholar]
  12. Seabright M. A rapid banding technique for human chromosomes. Lancet. 1971 Oct 30;2(7731):971–972. doi: 10.1016/s0140-6736(71)90287-x. [DOI] [PubMed] [Google Scholar]
  13. Seabright M. The use of proteolytic enzymes for the mapping of structural rearrangements in the chromosomes of man. Chromosoma. 1972;36(2):204–210. doi: 10.1007/BF00285214. [DOI] [PubMed] [Google Scholar]
  14. Sparkes R. S., Carrel R. E., Wright S. W. Absent thumbs with a ring D2 chromosome: a new deletion syndrome. Am J Hum Genet. 1967 Sep;19(5):644–659. [PMC free article] [PubMed] [Google Scholar]
  15. Taylor A. I. Dq-, Dr and retinoblastoma. Humangenetik. 1970;10(3):209–217. doi: 10.1007/BF00295782. [DOI] [PubMed] [Google Scholar]
  16. Wilson M. G., Melnyk J., Towner J. W. Retinoblastoma and deletion D (14) syndrome. J Med Genet. 1969 Sep;6(3):322–327. doi: 10.1136/jmg.6.3.322. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

RESOURCES