Literature DB >> 9783708

Mosaic supernumerary ring chromosome 19 identified by comparative genomic hybridisation.

S R Ghaffari1, E Boyd, J M Connor, A M Jones, J L Tolmie.   

Abstract

We report the use of comparative genomic hybridisation (CGH) to define the origin of a supernumerary ring chromosome which conventional cytogenetic banding and fluorescence in situ hybridisation (FISH) methods had failed to identify. Targeted FISH using whole chromosome 19 library arm and site specific probes then confirmed the CGH results. This study shows the feasibility of using CGH for the identification of supernumerary marker chromosomes, even in fewer than 50% of cells, where no clinical or cytogenetic clues are present.

Mesh:

Year:  1998        PMID: 9783708      PMCID: PMC1051460          DOI: 10.1136/jmg.35.10.836

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  27 in total

Review 1.  Duplication of distal 19q: clinical report and review.

Authors:  E Boyd; F S Grass; J C Parke; K Knutson; R E Stevenson
Journal:  Am J Med Genet       Date:  1992-02-01

2.  Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics.

Authors:  N P Carter; M A Ferguson-Smith; M T Perryman; H Telenius; A H Pelmear; M A Leversha; M T Glancy; S L Wood; K Cook; H M Dyson
Journal:  J Med Genet       Date:  1992-05       Impact factor: 6.318

3.  Chromosome-band-specific painting: chromosome in situ suppression hybridization using PCR products from a microdissected chromosome band as a probe pool.

Authors:  H X Deng; K Yoshiura; R W Dirks; N Harada; T Hirota; K Tsukamoto; Y Jinno; N Niikawa
Journal:  Hum Genet       Date:  1992-04       Impact factor: 4.132

4.  Partial trisomy for 19q due to paternal 17/19 reciprocal translocation.

Authors:  H Madokoro; S Ohdo; T Sonoda; K Kawaguchi; K Ohba
Journal:  Jinrui Idengaku Zasshi       Date:  1988-03

5.  Forty four probands with an additional "marker" chromosome.

Authors:  K E Buckton; G Spowart; M S Newton; H J Evans
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

6.  19q distal trisomy due to a de novo (19;22)(q13.2;p11) translocation.

Authors:  F Rivas; D García-Cruz; H Rivera; M L Plascencia; R M González; J M Cantú
Journal:  Ann Genet       Date:  1985

7.  Distal 19q duplication.

Authors:  J Zonana; M G Brown; R E Magenis
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

8.  Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors.

Authors:  A Kallioniemi; O P Kallioniemi; D Sudar; D Rutovitz; J W Gray; F Waldman; D Pinkel
Journal:  Science       Date:  1992-10-30       Impact factor: 47.728

9.  Trisomy for the distal third of the long arm of chromosome 19 in brother and sister.

Authors:  W Schmid
Journal:  Hum Genet       Date:  1979-02-15       Impact factor: 4.132

10.  A non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in man.

Authors:  J A Crolla; N R Dennis; P A Jacobs
Journal:  J Med Genet       Date:  1992-10       Impact factor: 6.318

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  1 in total

1.  "Familial" versus "sporadic" intellectual disability: contribution of subtelomeric rearrangements.

Authors:  Maryam Rafati; Mohammad R Ghadirzadeh; Yaser Heshmati; Homeira Adibi; Zarrintaj Keihanidoust; Mohammad R Eshraghian; Jila Dastan; Azadeh Hoseini; Marzieh Purhoseini; Saeed R Ghaffari
Journal:  Mol Cytogenet       Date:  2012-01-19       Impact factor: 2.009

  1 in total

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