Skip to main content
Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1994 Aug;31(8):585–594. doi: 10.1136/jmg.31.8.585

Inv dup(15) supernumerary marker chromosomes.

T Webb 1
PMCID: PMC1050018  PMID: 7815414

Full text

PDF
585

Selected References

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

  1. Buckton K. E., Spowart G., Newton M. S., Evans H. J. Forty four probands with an additional "marker" chromosome. Hum Genet. 1985;69(4):353–370. doi: 10.1007/BF00291656. [DOI] [PubMed] [Google Scholar]
  2. Callen D. F., Eyre H., Yip M. Y., Freemantle J., Haan E. A. Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes. Am J Med Genet. 1992 Jul 1;43(4):709–715. doi: 10.1002/ajmg.1320430412. [DOI] [PubMed] [Google Scholar]
  3. Chamberlin J., Magenis R. E. Parental origin of de novo chromosome rearrangements. Hum Genet. 1980;53(3):343–347. doi: 10.1007/BF00287054. [DOI] [PubMed] [Google Scholar]
  4. Friedrich U., Nielsen J. Bisatellited extra small metacentric chromosome in newborns. Clin Genet. 1974;6(1):23–31. doi: 10.1111/j.1399-0004.1974.tb00626.x. [DOI] [PubMed] [Google Scholar]
  5. Fujita H., Sakamoto Y., Hamamoto Y. An extra idic(15p)(q11) chromosome in Prader-Willi syndrome. Hum Genet. 1980;55(3):409–411. doi: 10.1007/BF00290227. [DOI] [PubMed] [Google Scholar]
  6. Gilmore D. H., Boyd E., McClure J. P., Batstone P., Connor J. M. Inv dup (15) with mental retardation but few dysmorphic features. J Med Genet. 1984 Jun;21(3):221–223. doi: 10.1136/jmg.21.3.221. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Goh K., Herrmann M. A., Campbell R. G., Thompson D. Abnormal chromosome in Prader-Willi syndrome. Clin Genet. 1984 Dec;26(6):597–601. doi: 10.1111/j.1399-0004.1984.tb01110.x. [DOI] [PubMed] [Google Scholar]
  8. Hoo J. J. High resolution pattern of an inverted duplication (15). Clin Genet. 1986 Mar;29(3):241–245. doi: 10.1111/j.1399-0004.1986.tb00818.x. [DOI] [PubMed] [Google Scholar]
  9. Kaplan L. C., Wharton R., Elias E., Mandell F., Donlon T., Latt S. A. Clinical heterogeneity associated with deletions in the long arm of chromosome 15: report of 3 new cases and their possible genetic significance. Am J Med Genet. 1987 Sep;28(1):45–53. doi: 10.1002/ajmg.1320280107. [DOI] [PubMed] [Google Scholar]
  10. Kirkilionis A. J., Sergovich F. R. Supernumary marker chromosomes in a mentally retarded population identified as inv dup(15). Clin Genet. 1987 Jun;31(6):425–428. doi: 10.1111/j.1399-0004.1987.tb02837.x. [DOI] [PubMed] [Google Scholar]
  11. Knight L. A., Lipson M., Mann J., Bachman R. Mosaic inversion duplication of chromosome 15 without phenotypic effect: occurrence in a father and daughter. Am J Med Genet. 1984 Mar;17(3):649–654. doi: 10.1002/ajmg.1320170315. [DOI] [PubMed] [Google Scholar]
  12. Knoll J. H., Nicholls R. D., Magenis R. E., Graham J. M., Jr, Lalande M., Latt S. A. Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion. Am J Med Genet. 1989 Feb;32(2):285–290. doi: 10.1002/ajmg.1320320235. [DOI] [PubMed] [Google Scholar]
  13. Kousseff B. G., Diamond T., Essig Y., Miller K., Tedesco T. Unique mosaicism in Prader-Labhart-Willi syndrome--a contiguous gene or aneuploidy syndrome? Am J Med Genet. 1987 Dec;28(4):803–811. doi: 10.1002/ajmg.1320280404. [DOI] [PubMed] [Google Scholar]
  14. Kousseff B. G. The cytogenetic controversy in the Prader-Labhart-Willi syndrome. Am J Med Genet. 1982 Dec;13(4):431–439. doi: 10.1002/ajmg.1320130412. [DOI] [PubMed] [Google Scholar]
  15. Kuwano A., Mutirangura A., Dittrich B., Buiting K., Horsthemke B., Saitoh S., Niikawa N., Ledbetter S. A., Greenberg F., Chinault A. C. Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis. Hum Mol Genet. 1992 Sep;1(6):417–425. doi: 10.1093/hmg/1.6.417. [DOI] [PubMed] [Google Scholar]
  16. Lazarus A. L., Moore K. E., Spinner N. B. Recurrent neuroleptic malignant syndrome associated with inv dup(15) and mental retardation. Clin Genet. 1991 Jan;39(1):65–67. doi: 10.1111/j.1399-0004.1991.tb02987.x. [DOI] [PubMed] [Google Scholar]
  17. Ledbetter D. H., Mascarello J. T., Riccardi V. M., Harper V. D., Airhart S. D., Strobel R. J. Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases. Am J Hum Genet. 1982 Mar;34(2):278–285. [PMC free article] [PubMed] [Google Scholar]
  18. Ledbetter D. H., Riccardi V. M., Airhart S. D., Strobel R. J., Keenan B. S., Crawford J. D. Deletions of chromosome 15 as a cause of the Prader-Willi syndrome. N Engl J Med. 1981 Feb 5;304(6):325–329. doi: 10.1056/NEJM198102053040604. [DOI] [PubMed] [Google Scholar]
  19. Malcolm S., Clayton-Smith J., Nichols M., Robb S., Webb T., Armour J. A., Jeffreys A. J., Pembrey M. E. Uniparental paternal disomy in Angelman's syndrome. Lancet. 1991 Mar 23;337(8743):694–697. doi: 10.1016/0140-6736(91)90278-w. [DOI] [PubMed] [Google Scholar]
  20. Manenti E. Two extra inv dup(15) chromosomes and male infertility: second case. Am J Med Genet. 1992 Feb 1;42(3):402–403. doi: 10.1002/ajmg.1320420337. [DOI] [PubMed] [Google Scholar]
  21. Maraschio P., Zuffardi O., Bernardi F., Bozzola M., De Paoli C., Fonatsch C., Flatz S. D., Ghersini L., Gimelli G., Loi M. Preferential maternal derivation in inv dup(15): analysis of eight new cases. Hum Genet. 1981;57(4):345–350. doi: 10.1007/BF00281681. [DOI] [PubMed] [Google Scholar]
  22. Martín-Lucas M. A., Pérez-Castillo A., Abrisqueta J. A. Infertility associated with two accessory bisatellited chromosomes. Hum Genet. 1986 Jun;73(2):133–136. doi: 10.1007/BF00291603. [DOI] [PubMed] [Google Scholar]
  23. Mattei J. F., Mattei M. G., Giraud F. Prader-Willi syndrome and chromosome 15. A clinical discussion of 20 cases. Hum Genet. 1983;64(4):356–362. doi: 10.1007/BF00292367. [DOI] [PubMed] [Google Scholar]
  24. Med K., Kosinková A., Havlícek K. První zkusenosti s pouzitím fibrinového lepidla v lécbe akutního krvácení do gastroduodena. Rozhl Chir. 1992 Dec;71(12):671–676. [PubMed] [Google Scholar]
  25. Michaelsen K. F., Lundsteen C., Hansen F. J. Prader-Willi syndrome and chromosomal mosaicism 46,XY/47,XY,+mar in two cases. Clin Genet. 1979 Sep;16(3):147–150. doi: 10.1111/j.1399-0004.1979.tb00983.x. [DOI] [PubMed] [Google Scholar]
  26. Miny P., Basaran S., Kuwertz E., Holzgreve W., Pawlowitzki I. H. Inv dup (15): prenatal diagnosis and postnatal follow-up. Prenat Diagn. 1986 Jul-Aug;6(4):303–306. doi: 10.1002/pd.1970060411. [DOI] [PubMed] [Google Scholar]
  27. Mohandas T., Canning N., Chu W., Passage M. B., Anderson C. E., Kaback M. M. Marker chromosomes: cytogenetic characterization and implications for prenatal diagnosis. Am J Med Genet. 1985 Feb;20(2):361–368. doi: 10.1002/ajmg.1320200220. [DOI] [PubMed] [Google Scholar]
  28. Narahara K., Hiramoto K., Murakami M., Miyake S., Tsuji K., Yokoyama Y., Namba H., Ninomiya S., Murakami R., Seino Y. Unique karyotypes in two patients with Prader-Willi syndrome. Am J Med Genet. 1992 Mar 1;42(5):671–677. doi: 10.1002/ajmg.1320420509. [DOI] [PubMed] [Google Scholar]
  29. Nicholls R. D., Knoll J. H., Butler M. G., Karam S., Lalande M. Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome. Nature. 1989 Nov 16;342(6247):281–285. doi: 10.1038/342281a0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Nicholls R. D., Knoll J. H., Glatt K., Hersh J. H., Brewster T. D., Graham J. M., Jr, Wurster-Hill D., Wharton R., Latt S. A. Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndrome. Am J Med Genet. 1989 May;33(1):66–77. doi: 10.1002/ajmg.1320330109. [DOI] [PubMed] [Google Scholar]
  31. Plattner R., Heerema N. A., Howard-Peebles P. N., Miles J. H., Soukup S., Palmer C. G. Clinical findings in patients with marker chromosomes identified by fluorescence in situ hybridization. Hum Genet. 1993 Jul;91(6):589–598. doi: 10.1007/BF00205086. [DOI] [PubMed] [Google Scholar]
  32. Plattner R., Heerema N. A., Patil S. R., Howard-Peebles P. N., Palmer C. G. Characterization of seven DA/DAPI-positive bisatellited marker chromosomes by in situ hybridization. Hum Genet. 1991 Jul;87(3):290–296. doi: 10.1007/BF00200906. [DOI] [PubMed] [Google Scholar]
  33. Rauch A., Pfeiffer R. A., Trautmann U., Liehr T., Rott H. D., Ulmer R. A study of ten small supernumerary (marker) chromosomes identified by fluorescence in situ hybridization (FISH). Clin Genet. 1992 Aug;42(2):84–90. doi: 10.1111/j.1399-0004.1992.tb03145.x. [DOI] [PubMed] [Google Scholar]
  34. Ridler M. A., Garrod O., Berg J. M. A case of Prader-Willi syndrome in a girl with a small extra chromosome. Acta Paediatr Scand. 1971 Mar;60(2):222–226. doi: 10.1111/j.1651-2227.1971.tb06646.x. [DOI] [PubMed] [Google Scholar]
  35. Robinson W. P., Binkert F., Giné R., Vazquez C., Müller W., Rosenkranz W., Schinzel A. Clinical and molecular analysis of five inv dup(15) patients. Eur J Hum Genet. 1993;1(1):37–50. doi: 10.1159/000472386. [DOI] [PubMed] [Google Scholar]
  36. Robinson W. P., Bottani A., Xie Y. G., Balakrishman J., Binkert F., Mächler M., Prader A., Schinzel A. Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients. Am J Hum Genet. 1991 Dec;49(6):1219–1234. [PMC free article] [PubMed] [Google Scholar]
  37. Robinson W. P., Wagstaff J., Bernasconi F., Baccichetti C., Artifoni L., Franzoni E., Suslak L., Shih L. Y., Aviv H., Schinzel A. A. Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup(15) chromosome. J Med Genet. 1993 Sep;30(9):756–760. doi: 10.1136/jmg.30.9.756. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Schmid M., Schindler D., Haaf T. Structure, origin and effects of a supernumerary marker chromosome 15. Clin Genet. 1986 Jul;30(1):63–71. doi: 10.1111/j.1399-0004.1986.tb00570.x. [DOI] [PubMed] [Google Scholar]
  39. Schreck R. R., Breg W. R., Erlanger B. F., Miller O. J. Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15. Hum Genet. 1977 Apr 7;36(1):1–12. doi: 10.1007/BF00390430. [DOI] [PubMed] [Google Scholar]
  40. Shibuya Y., Tonoki H., Kajii N., Niikawa N. Identification of a marker chromosome as inv dup(15) by molecular analysis. Clin Genet. 1991 Sep;40(3):233–236. doi: 10.1111/j.1399-0004.1991.tb03083.x. [DOI] [PubMed] [Google Scholar]
  41. Steinbach P., Djalali M., Hansmann I., Kattner E., Meisel-Stosiek M., Probeck H. D., Schmidt A., Wolf M. The genetic significance of accessory bisatellited marker chromosomes. Hum Genet. 1983;65(2):155–164. doi: 10.1007/BF00286654. [DOI] [PubMed] [Google Scholar]
  42. Stetten G., Sroka-Zaczek B., Corson V. L. Prenatal detection of an accessory chromosome identified as an inversion duplication (15). Hum Genet. 1981;57(4):357–359. doi: 10.1007/BF00281684. [DOI] [PubMed] [Google Scholar]
  43. Van Dyke D. L., Weiss L., Logan M., Pai G. S. The origin and behavior of two isodicentric bisatellited chromosomes. Am J Hum Genet. 1977 May;29(3):294–300. [PMC free article] [PubMed] [Google Scholar]
  44. Wahlström J., Steffenburg S., Hellgren L., Gillberg C. Chromosome findings in twins with early-onset autistic disorder. Am J Med Genet. 1989 Jan;32(1):19–21. doi: 10.1002/ajmg.1320320105. [DOI] [PubMed] [Google Scholar]
  45. Wisniewski L. P., Doherty R. A. Supernumerary microchromosomes identified as inverted duplications of chromosome 15: a report of three cases. Hum Genet. 1985;69(2):161–163. doi: 10.1007/BF00293289. [DOI] [PubMed] [Google Scholar]
  46. Wisniewski L. P., Witt M. E., Ginsberg-Fellner F., Wilner J., Desnick R. J. Prader-Willi syndrome and a bisatellited derivative of chromosome 15. Clin Genet. 1980 Jul;18(1):42–47. doi: 10.1111/j.1399-0004.1980.tb01363.x. [DOI] [PubMed] [Google Scholar]
  47. Wisniewski L., Hassold T., Heffelfinger J., Higgins J. V. Cytogenetic and clinical studies in five cases of inv dup(15). Hum Genet. 1979 Sep;50(3):259–270. doi: 10.1007/BF00399391. [DOI] [PubMed] [Google Scholar]
  48. Wulfsberg E. A., Sparkes R. S., Klisak I. J., Gurfield W. B. A 15 leads to 1 translocation in a patient mosaic for presence or absence of an isodic(15p)(q11). Am J Med Genet. 1982 Dec;13(4):417–421. doi: 10.1002/ajmg.1320130410. [DOI] [PubMed] [Google Scholar]
  49. Yip M. Y., Mark J., Hultén M. Supernumerary chromosomes in six patients. Clin Genet. 1982 Jun;21(6):397–406. doi: 10.1111/j.1399-0004.1982.tb01394.x. [DOI] [PubMed] [Google Scholar]
  50. Zannotti M., Preto A., Giovanardi P. R., Dallapiccola B. Extra dicentric 15 pter leads to q21/22 chromosomes in five unrelated patients with a distinct syndrome of progressive psychomotor retardation, seizures, hyper-reactivity and dermatoglyphic abnormalities. J Ment Defic Res. 1980 Dec;24(Pt 4):235–242. doi: 10.1111/j.1365-2788.1980.tb00077.x. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Medical Genetics are provided here courtesy of BMJ Publishing Group

RESOURCES