Home LiteratureArticle Details
PMID: 7815414 Published · ppublish English Journal Article Review

Inv dup(15) supernumerary marker chromosomes.

Journal of medical genetics ·Vol. 31 ·No. 8 ·1994-08-00 ·Pages 585-94

Webb T

Abstract

暂无摘要

MeSH Terms
Abnormalities, Multiple/genetics Aneuploidy Chromosome Aberrations/diagnosis,epidemiology,genetics Chromosome Disorders Chromosome Inversion Chromosomes, Human, Pair 15/ultrastructure Fetal Diseases/diagnosis,genetics Genomic Imprinting Humans In Situ Hybridization, Fluorescence Incidence Intellectual Disability/genetics Karyotyping Mosaicism Phenotype Prader-Willi Syndrome/genetics Prenatal Diagnosis
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Webb T
Department of Clinical Genetics, Birmingham Maternity Hospital, Edgbaston, Birmingham.
References (50)
50 references, click to expand
  1. Characterization of seven DA/DAPI-positive bisatellited marker chromosomes by in situ hybridization.
    Hum Genet. 1991 Jul;87(3):290-6 PMID: 1864603
  2. Clinical and molecular analysis of five inv dup(15) patients.
    Eur J Hum Genet. 1993;1(1):37-50 PMID: 8069650
  3. Identification of a marker chromosome as inv dup(15) by molecular analysis.
    Clin Genet. 1991 Sep;40(3):233-6 PMID: 1685358
  4. Two extra inv dup(15) chromosomes and male infertility: second case.
    Am J Med Genet. 1992 Feb 1;42(3):402-3 PMID: 1536192
  5. A case of Prader-Willi syndrome in a girl with a small extra chromosome.
    Acta Paediatr Scand. 1971 Mar;60(2):222-6 PMID: 5548129
  6. Bisatellited extra small metacentric chromosome in newborns.
    Clin Genet. 1974;6(1):23-31 PMID: 4426127
  7. Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15.
    Hum Genet. 1977 Apr 7;36(1):1-12 PMID: 323137
  8. The origin and behavior of two isodicentric bisatellited chromosomes.
    Am J Hum Genet. 1977 May;29(3):294-300 PMID: 868876
  9. Prader-Willi syndrome and chromosomal mosaicism 46,XY/47,XY,+mar in two cases.
    Clin Genet. 1979 Sep;16(3):147-50 PMID: 573673
  10. Cytogenetic and clinical studies in five cases of inv dup(15).
    Hum Genet. 1979 Sep;50(3):259-70 PMID: 489010
  11. Parental origin of de novo chromosome rearrangements.
    Hum Genet. 1980;53(3):343-7 PMID: 6445322
  12. Prader-Willi syndrome and a bisatellited derivative of chromosome 15.
    Clin Genet. 1980 Jul;18(1):42-7 PMID: 7418253
  13. Deletions of chromosome 15 as a cause of the Prader-Willi syndrome.
    N Engl J Med. 1981 Feb 5;304(6):325-9 PMID: 7442771
  14. An extra idic(15p)(q11) chromosome in Prader-Willi syndrome.
    Hum Genet. 1980;55(3):409-11 PMID: 6162774
  15. 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 4:235-42 PMID: 7218339
  16. Preferential maternal derivation in inv dup(15): analysis of eight new cases.
    Hum Genet. 1981;57(4):345-50 PMID: 7286973
  17. Prenatal detection of an accessory chromosome identified as an inversion duplication (15).
    Hum Genet. 1981;57(4):357-9 PMID: 7286975
  18. Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases.
    Am J Hum Genet. 1982 Mar;34(2):278-85 PMID: 7072717
  19. Supernumerary chromosomes in six patients.
    Clin Genet. 1982 Jun;21(6):397-406 PMID: 6957276
  20. 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):417-21 PMID: 7158641
  21. The cytogenetic controversy in the Prader-Labhart-Willi syndrome.
    Am J Med Genet. 1982 Dec;13(4):431-9 PMID: 7158643
  22. Prader-Willi syndrome and chromosome 15. A clinical discussion of 20 cases.
    Hum Genet. 1983;64(4):356-62 PMID: 6618488
  23. The genetic significance of accessory bisatellited marker chromosomes.
    Hum Genet. 1983;65(2):155-64 PMID: 6228512
  24. Mosaic inversion duplication of chromosome 15 without phenotypic effect: occurrence in a father and daughter.
    Am J Med Genet. 1984 Mar;17(3):649-54 PMID: 6585144
  25. Inv dup (15) with mental retardation but few dysmorphic features.
    J Med Genet. 1984 Jun;21(3):221-3 PMID: 6748020
  26. Abnormal chromosome in Prader-Willi syndrome.
    Clin Genet. 1984 Dec;26(6):597-601 PMID: 6499272
  27. Supernumerary microchromosomes identified as inverted duplications of chromosome 15: a report of three cases.
    Hum Genet. 1985;69(2):161-3 PMID: 3972417
  28. Marker chromosomes: cytogenetic characterization and implications for prenatal diagnosis.
    Am J Med Genet. 1985 Feb;20(2):361-8 PMID: 2579555
  29. Forty four probands with an additional "marker" chromosome.
    Hum Genet. 1985;69(4):353-70 PMID: 3857214
  30. High resolution pattern of an inverted duplication (15).
    Clin Genet. 1986 Mar;29(3):241-5 PMID: 3457663
  31. Infertility associated with two accessory bisatellited chromosomes.
    Hum Genet. 1986 Jun;73(2):133-6 PMID: 3459705
  32. Inv dup (15): prenatal diagnosis and postnatal follow-up.
    Prenat Diagn. 1986 Jul-Aug;6(4):303-6 PMID: 3748995
  33. Structure, origin and effects of a supernumerary marker chromosome 15.
    Clin Genet. 1986 Jul;30(1):63-71 PMID: 3463440
  34. Supernumary marker chromosomes in a mentally retarded population identified as inv dup(15).
    Clin Genet. 1987 Jun;31(6):425-8 PMID: 3621648
  35. 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 PMID: 3674117
  36. Unique mosaicism in Prader-Labhart-Willi syndrome--a contiguous gene or aneuploidy syndrome?
    Am J Med Genet. 1987 Dec;28(4):803-11 PMID: 3688018
  37. 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):285-90 PMID: 2564739
  38. Chromosome findings in twins with early-onset autistic disorder.
    Am J Med Genet. 1989 Jan;32(1):19-21 PMID: 2705478
  39. 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 PMID: 2568752
  40. Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.
    Nature. 1989 Nov 16;342(6247):281-5 PMID: 2812027
  41. Recurrent neuroleptic malignant syndrome associated with inv dup(15) and mental retardation.
    Clin Genet. 1991 Jan;39(1):65-7 PMID: 1997219
  42. Uniparental paternal disomy in Angelman's syndrome.
    Lancet. 1991 Mar 23;337(8743):694-7 PMID: 1672177
  43. Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes.
    Am J Med Genet. 1992 Jul 1;43(4):709-15 PMID: 1377870
  44. Unique karyotypes in two patients with Prader-Willi syndrome.
    Am J Med Genet. 1992 Mar 1;42(5):671-7 PMID: 1632436
  45. A study of ten small supernumerary (marker) chromosomes identified by fluorescence in situ hybridization (FISH).
    Clin Genet. 1992 Aug;42(2):84-90 PMID: 1424236
  46. [Initial experience with use of fibrin glue in the treatment of acute gastroduodenal hemorrhage].
    Rozhl Chir. 1992 Dec;71(12):671-6 PMID: 1485204
  47. Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis.
    Hum Mol Genet. 1992 Sep;1(6):417-25 PMID: 1363801
  48. Clinical findings in patients with marker chromosomes identified by fluorescence in situ hybridization.
    Hum Genet. 1993 Jul;91(6):589-98 PMID: 8340114
  49. 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):756-60 PMID: 8411071
  50. Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients.
    Am J Hum Genet. 1991 Dec;49(6):1219-34 PMID: 1684085
Article Info
Journal
Journal of medical genetics
Abbr.
J Med Genet
ISSN
0022-2593
DOI
10.1136/jmg.31.8.585
Published
1994-08-00
Pages
585-94
Language
English
Region
England
NLM ID
2985087R
PMCID
PMC1050018
Subset
IM
External Links
PubMed source DOI: 10.1136/jmg.31.8.585 PMC Full Text View journal details
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com

Copyright © 2026.Genelibs Jinan Honghui Biotechnology Co., Ltd. 鲁ICP备20007159号-2