Full text
PDF











Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Cross H. E., Hansen R. C., Morrow G., 3rd, Davis J. R. Retinoblastoma in a patient with a 13qXp translocation. Am J Ophthalmol. 1977 Oct;84(4):548–554. doi: 10.1016/0002-9394(77)90450-0. [DOI] [PubMed] [Google Scholar]
- Cuschieri A., Agius P. V., Scheres J. M. Partial deletion of the long arm of chromosome no. 13. Hum Genet. 1977 May 10;36(3):341–344. doi: 10.1007/BF00446286. [DOI] [PubMed] [Google Scholar]
- Francke U., Kung F. Sporadic bilateral retinoblastoma and 13q- chromosomal deletion. Med Pediatr Oncol. 1976;2(4):379–385. doi: 10.1002/mpo.2950020404. [DOI] [PubMed] [Google Scholar]
- Gey W. Dq-, multiple Missbildungen und Retinoblastom. Humangenetik. 1970;10(4):362–365. doi: 10.1007/BF00278776. [DOI] [PubMed] [Google Scholar]
- 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]
- Hashem N., Khalifa S. Retinoblastoma. A model of hereditary fragile chromosomal regions. Hum Hered. 1975;25(1):35–49. doi: 10.1159/000152706. [DOI] [PubMed] [Google Scholar]
- Howard-Peebles P. N., Yarbrough K. M., Stoddard G. R., Rary J. M. Translocation of 9q/13q resulting in duplication (trisomy 9pter leads to 9q22) and deficiency (monosomy 13pter leads to 13q12). Clin Genet. 1977 Jan;11(1):46–52. [PubMed] [Google Scholar]
- Howard R. O., Breg W. R., Albert D. M., Lesser R. L. Retinoblastoma and chromosome abnormality. Partial deletion of the long arm of chromosome 13. Arch Ophthalmol. 1974 Dec;92(6):490–493. doi: 10.1001/archopht.1974.01010010504007. [DOI] [PubMed] [Google Scholar]
- Ikeuchi T., Sonta S., Sasaki M., Hujita M., Tsunematsu K. Chromosome banding patterns in an infant with 13q minus syndrome. Humangenetik. 1974 Mar 28;21(4):309–314. doi: 10.1007/BF00273368. [DOI] [PubMed] [Google Scholar]
- Knudson A. G., Jr, Meadows A. T., Nichols W. W., Hill R. Chromosomal deletion and retinoblastoma. N Engl J Med. 1976 Nov 11;295(20):1120–1123. doi: 10.1056/NEJM197611112952007. [DOI] [PubMed] [Google Scholar]
- 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]
- Lejeune J. De la duplication de structures circulaires. Ann Genet. 1968 Jun;11(2):71–77. [PubMed] [Google Scholar]
- Mark J. Chromosomal analysis of a human retinoblastoma. Acta Ophthalmol (Copenh) 1970;48(1):124–135. doi: 10.1111/j.1755-3768.1970.tb06580.x. [DOI] [PubMed] [Google Scholar]
- Noel B., Quack B., Rethore M. O. Partial deletions and trisomies of chromosome 13; mapping of bands associated with particular malformations. Clin Genet. 1976 Jun;9(6):593–602. doi: 10.1111/j.1399-0004.1976.tb01618.x. [DOI] [PubMed] [Google Scholar]
- O'Grady R. B., Rothstein T. B., Romano P. E. D-group deletion syndromes and retinoblastoma. Am J Ophthalmol. 1974 Jan;77(1):40–45. doi: 10.1016/0002-9394(74)90602-3. [DOI] [PubMed] [Google Scholar]
- 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]
- Pathak S., Sinha A. K. An alternative model for ring chromosome perpetuation in a human subject. Ann Hum Genet. 1972 Apr;35(4):471–476. doi: 10.1111/j.1469-1809.1957.tb01872.x. [DOI] [PubMed] [Google Scholar]
- Pruett R. C., Atkins L. Chromosome studies in patients with retinoblastoma. Arch Ophthalmol. 1969 Aug;82(2):177–181. doi: 10.1001/archopht.1969.00990020179005. [DOI] [PubMed] [Google Scholar]
- Schwanitz G., Reither M., Grosse G., Hägele C., Grosse K-P, Gutfried U. Partial monosomy 13 as the result of a balanced translocation 3/13 pat. Humangenetik. 1975 Jun 19;28(2):93–96. doi: 10.1007/BF00735740. [DOI] [PubMed] [Google Scholar]
- 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]
- Suzuki Y., Ono K., Oka S., Matsubara T., Arima M., Nakagome Y. A case of (13q;18q) translocation with proximal 13q monosomy. Hum Genet. 1977 Oct 14;38(3):337–341. doi: 10.1007/BF00402161. [DOI] [PubMed] [Google Scholar]
- Taylor A. I. Dq-, Dr and retinoblastoma. Humangenetik. 1970;10(3):209–217. doi: 10.1007/BF00295782. [DOI] [PubMed] [Google Scholar]
- WIENER S., REESE A. B., HYMAN G. A. Chromosome studies in retinoblastoma. Arch Ophthalmol. 1963 Mar;69:311–313. doi: 10.1001/archopht.1963.00960040317009. [DOI] [PubMed] [Google Scholar]
- Weichselbaum R. R., Nove J., Little J. B. Skin fibroblasts from a D-deletion type retinoblastoma patient are abnormally X-ray sensitive. Nature. 1977 Apr 21;266(5604):726–727. doi: 10.1038/266726a0. [DOI] [PubMed] [Google Scholar]
- Wilson M. G., Ebbin A. J., Towner J. W., Spencer W. H. Chromosomal anomalies in patients with retinoblastoma. Clin Genet. 1977 Jul;12(1):1–8. doi: 10.1111/j.1399-0004.1977.tb00894.x. [DOI] [PubMed] [Google Scholar]
- 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]
- Wilson M. G., Towner J. W., Fujimoto A. Retinoblastoma and D-chromosome deletions. Am J Hum Genet. 1973 Jan;25(1):57–61. [PMC free article] [PubMed] [Google Scholar]
- Wilson M. G., Towner J. W., Fujimoto A. Retinoblastoma and D-chromosome deletions. Am J Hum Genet. 1973 Jan;25(1):57–61. [PMC free article] [PubMed] [Google Scholar]
- Yunis J. J., Ramsay N. Retinoblastoma and subband deletion of chromosome 13. Am J Dis Child. 1978 Feb;132(2):161–163. doi: 10.1001/archpedi.1978.02120270059012. [DOI] [PubMed] [Google Scholar]
- Zimmerman L. E. Changing concepts concerning the pathogenesis of infectious diseases. Am J Ophthalmol. 1970 Jun;69(6):947–964. doi: 10.1016/0002-9394(70)91038-x. [DOI] [PubMed] [Google Scholar]
