Skip to main content
NCBI home page
The British Journal of Ophthalmology logoLink to The British Journal of Ophthalmology
. 1994 May;78(5):415–417. doi: 10.1136/bjo.78.5.415

Trisomy 4p and ocular defects.

I W Lurie 1, V A Samochvalov 1
PMCID: PMC504802  PMID: 8025082

Full text

PDF
415

Selected References

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

  1. Andersen O., Lundsteen C., Niebuhr E. A complex four-break rearrangement between chromosomes 4 and 13 resulting in a recombinant chromosome 4. Cytogenet Cell Genet. 1981;30(1):3–10. doi: 10.1159/000131581. [DOI] [PubMed] [Google Scholar]
  2. Dallapiccola B., Mastroiacovo P. P., Montali E., Sommer A. Trisomy 4p: five new observations and overview. Clin Genet. 1977 Dec;12(6):344–356. doi: 10.1111/j.1399-0004.1977.tb00953.x. [DOI] [PubMed] [Google Scholar]
  3. Giraud F., Mattei J. F., Mattei M. G., Ayme S., Bernard R. La trisomie 4p. A propos de 3 observations. Humangenetik. 1975 Nov 6;30(2):99–108. doi: 10.1007/BF00291941. [DOI] [PubMed] [Google Scholar]
  4. Goggin M., O'Keefe M., Hughes H. Two cases of coloboma associated with unbalanced translocations. Br J Ophthalmol. 1993 Feb;77(2):122–123. doi: 10.1136/bjo.77.2.122. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Hersh J. H., Dale K. S., Gerald P. S., Yen F. F., Weisskopf B., Dinno N. D. Dup(4p)del(9p) in a familial mental retardation syndrome. Resemblance to de Lange syndrome detected by high-resolution banding. Am J Dis Child. 1985 Jan;139(1):81–84. doi: 10.1001/archpedi.1985.02140030087037. [DOI] [PubMed] [Google Scholar]
  6. Herva R., von Wendt L. De novo trisomy 4pter leads to q21. Hum Genet. 1978 Mar 17;41(2):225–230. doi: 10.1007/BF00273105. [DOI] [PubMed] [Google Scholar]
  7. Hirsch B., Baldinger S. Pericentric inversion of chromosome 4 giving rise to dup(4p) and dup(4q) recombinants within a single kindred. Am J Med Genet. 1993 Jan 1;45(1):5–8. doi: 10.1002/ajmg.1320450104. [DOI] [PubMed] [Google Scholar]
  8. Hoo J. J., Fuhrmann-Rieger A., Foerster W., Doppl W., Pascu F., Bauer J. Multiple Fehlbildungen als Folge von partieller Trisomie 4p und partieller Monosomie 18q durch meiotische Rekombination. Monatsschr Kinderheilkd. 1983 Mar;131(3):169–172. [PubMed] [Google Scholar]
  9. Kessel E., Pfeiffer R. A., Kosenow W. Der Phänotyp der Trisomie des kurzen Arms eines Chromosoms Nr.4 (Ein neuer Fall mit t (4 p; 11 q) Klin Padiatr. 1976 May;188(3):215–219. [PubMed] [Google Scholar]
  10. Kleczkowska A., Fryns J. P., van den Berghe H. Trisomy of the short arm of chromosome 4: the changing phenotype with age. Ann Genet. 1992;35(4):217–223. [PubMed] [Google Scholar]
  11. Mayer U. M., Bialasiewicz A. A. Ocular findings in a 4 p- deletion syndrome (Wolf-Hirschhorn). Ophthalmic Paediatr Genet. 1989 Mar;10(1):69–72. doi: 10.3109/13816818909083777. [DOI] [PubMed] [Google Scholar]
  12. Mortimer J. G., Chewings W. E., Gardner R. J. A further report on a kindred with cases of 4p trisomy and monosomy. Hum Hered. 1980;30(1):58–61. doi: 10.1159/000153091. [DOI] [PubMed] [Google Scholar]
  13. Narahara K., Himoto Y., Yokoyama Y., Kasai R., Hata A., Kikkawa K., Takahashi Y., Wakita Y., Kimura S., Kimoto H. The critical monosomic segment involved in 4p- syndrome: a high-resolution banding study on five inherited cases. Jinrui Idengaku Zasshi. 1984 Dec;29(4):403–413. doi: 10.1007/BF01876498. [DOI] [PubMed] [Google Scholar]
  14. Rethoré M. O., Dutrillaux B., Job J. C., Lejeune J. Trisomie 4p par aneusomie de recombinaison d'une inv(4)(p14q35) Ann Genet. 1974 Jun;17(2):109–114. [PubMed] [Google Scholar]
  15. Schinzel A., D'Apuzzo V. Anophthalmia in a retarded girl with partial trisomy 4p and 22 following a maternal translocation, rcp(4;22)(p15.2;q11.2). Ophthalmic Paediatr Genet. 1990 Jun;11(2):139–142. doi: 10.3109/13816819009012960. [DOI] [PubMed] [Google Scholar]
  16. Wiegand W. Augenveränderungen bei partieller Trisomie 4p. Fortschr Ophthalmol. 1986;83(3):317–319. [PubMed] [Google Scholar]
  17. Wilson M. G., Towner J. W., Coffin G. S., Ebbin A. J., Siris E., Brager P. Genetic and clinical studies in 13 patients with the Wolf-Hirschhorn syndrome [del(4p)]. Hum Genet. 1981;59(4):297–307. doi: 10.1007/BF00295461. [DOI] [PubMed] [Google Scholar]
  18. Wilson M. G., Towner J. W., Coffin G. S., Forsman I. Inherited pericentric inversion of chromosome no. 4. Am J Hum Genet. 1970 Nov;22(6):679–690. [PMC free article] [PubMed] [Google Scholar]
  19. Wyandt H. E., Milunsky J., Lerner T., Gusella J. F., Hou A., MacDonald M., Adekunle S., Milunsky A. Characterization of a duplication in the terminal band of 4p by molecular cytogenetics. Am J Med Genet. 1993 Apr 1;46(1):72–76. doi: 10.1002/ajmg.1320460112. [DOI] [PubMed] [Google Scholar]
  20. Zierler H., Behmel A., Rosenkranz W. Klinische Bedeutung chromosomaler Translokationen. Wien Klin Wochenschr. 1980;92(11):395–405. [PubMed] [Google Scholar]

Articles from The British Journal of Ophthalmology are provided here courtesy of BMJ Publishing Group

RESOURCES