Literature DB >> 589849

C-bands in seven cases of accessory small chromosomes.

D Soudek, H Sroka.   

Abstract

The C-bands of two cases of familial, genetically inactive, accessory small chromosomes and five cases of genetically active chromosomes were examined. Inactive chromosomes consist of constitutive heterochromatin and satellites only. In active chromosomes, euchromatin was present. These chromosomes contained two, one or no C-bands, although all these chromosomes were morphologically monocentric. C-banding is more informative than other banding methods for this category of chromosomes.

Mesh:

Year:  1977        PMID: 589849     DOI: 10.1111/j.1399-0004.1977.tb00942.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  8 in total

1.  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

2.  Characterization of supernumerary ring marker chromosomes by fluorescence in situ hybridization (FISH).

Authors:  E Blennow; G Annerén; T H Bui; E Berggren; E Asadi; M Nordenskjöld
Journal:  Am J Hum Genet       Date:  1993-08       Impact factor: 11.025

3.  The genetic significance of accessory bisatellited marker chromosomes.

Authors:  P Steinbach; M Djalali; I Hansmann; E Kattner; M Meisel-Stosiek; H D Probeck; A Schmidt; M Wolf
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

4.  Complex chromosomal rearrangement leading to partial trisomy 22.

Authors:  I L Hansteen; L Schirmer; S Hestetun; A Brøgger
Journal:  J Med Genet       Date:  1980-02       Impact factor: 6.318

5.  Prenatal detection of an accessory chromosome identified as an inversion duplication (15).

Authors:  G Stetten; B Sroka-Zaczek; V L Corson
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

6.  Incidence and significance of supernumerary marker chromosomes in prenatal diagnosis.

Authors:  P A Benn; L Y Hsu
Journal:  Am J Hum Genet       Date:  1984-09       Impact factor: 11.025

Review 7.  Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.

Authors:  M G Mattei; N Souiah; J F Mattei
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

8.  A fragile X suppressor in the normal human blood?

Authors:  D Soudek; M Emanuel
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

  8 in total

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