Literature DB >> 1864603

Characterization of seven DA/DAPI-positive bisatellited marker chromosomes by in situ hybridization.

R Plattner1, N A Heerema, S R Patil, P N Howard-Peebles, C G Palmer.   

Abstract

Seven dicentric bisatellited marker chromosomes, ascertained at amniocentesis, chorionic villus sampling, and in blood from an abnormal liveborn were characterized cytogenetically. All seven markers demonstrated brilliant bands by the DA/DAPI technique corresponding to C-band positive regions. Although some dicentric DA/DAPI-positive bisatellited markers have been identified as inverted duplicated 15s, recent literature has suggested that DA/DAPI lacks specificity for chromosome 15. Our evaluation of DA/DAPI-positive bisatellited marker chromosomes by in situ hybridization shows that some originate from chromosome 15 whereas DA/DAPI negative bisatellited markers may not be derived from 15. The morphological variations noted in our studies are discussed with respect to nomenclature.

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Year:  1991        PMID: 1864603     DOI: 10.1007/bf00200906

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  30 in total

1.  Evidence for lack of specificity of the DA/DAPI technique.

Authors:  A Pérez-Castillo; M A Martín-Lucas; J A Abrisqueta
Journal:  Cytogenet Cell Genet       Date:  1987

2.  Intensity heteromorphisms of human chromosome 15p by DA/DAPI technique.

Authors:  A Babu; M J Macera; R S Verma
Journal:  Hum Genet       Date:  1986-08       Impact factor: 4.132

3.  Organization of a repetitive human 1.8 kb KpnI sequence localized in the heterochromatin of chromosome 15.

Authors:  M J Higgins; H S Wang; I Shtromas; T Haliotis; J C Roder; J J Holden; B N White
Journal:  Chromosoma       Date:  1985       Impact factor: 4.316

4.  18p- syndrome: an unusual case and diagnosis by in situ hybridization with chromosome 18-specific alphoid DNA sequence.

Authors:  S G Vorsanova; Y B Yurov; I A Alexandrov; I A Demidova; S P Mitkevich; A F Tirskaia
Journal:  Hum Genet       Date:  1986-02       Impact factor: 4.132

5.  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

6.  "A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum.

Authors:  A P Feinberg; B Vogelstein
Journal:  Anal Biochem       Date:  1984-02       Impact factor: 3.365

7.  A simple method of reducing the fading of immunofluorescence during microscopy.

Authors:  G D Johnson; G M Nogueira Araujo
Journal:  J Immunol Methods       Date:  1981       Impact factor: 2.303

8.  Prader-Willi syndrome and a bisatellited derivative of chromosome 15.

Authors:  L P Wisniewski; M E Witt; F Ginsberg-Fellner; J Wilner; R J Desnick
Journal:  Clin Genet       Date:  1980-07       Impact factor: 4.438

9.  Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16.

Authors:  D F Callen; M L Ringenbergs; J C Fowler; C J Freemantle; E A Haan
Journal:  J Med Genet       Date:  1990-03       Impact factor: 6.318

10.  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.

Authors:  M Zannotti; A Preto; P R Giovanardi; B Dallapiccola
Journal:  J Ment Defic Res       Date:  1980-12
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  8 in total

1.  Large inv dup(15) chromosome in two generations.

Authors:  J J Van Der Smagt; J C Giltay; J J De Ne; G H Slabbers
Journal:  J Med Genet       Date:  1996-03       Impact factor: 6.318

2.  Update and Review: Supernumerary Marker Chromosomes.

Authors:  S Ungerleider
Journal:  J Genet Couns       Date:  2000-08       Impact factor: 2.537

Review 3.  Inv dup(15) supernumerary marker chromosomes.

Authors:  T Webb
Journal:  J Med Genet       Date:  1994-08       Impact factor: 6.318

4.  Clinical findings in patients with marker chromosomes identified by fluorescence in situ hybridization.

Authors:  R Plattner; N A Heerema; P N Howard-Peebles; J H Miles; S Soukup; C G Palmer
Journal:  Hum Genet       Date:  1993-07       Impact factor: 4.132

5.  Molecular cytogenetic evidence for a common breakpoint in the largest inverted duplications of chromosome 15.

Authors:  A E Wandstrat; J Leana-Cox; L Jenkins; S Schwartz
Journal:  Am J Hum Genet       Date:  1998-04       Impact factor: 11.025

6.  Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications.

Authors:  J Leana-Cox; L Jenkins; C G Palmer; R Plattner; L Sheppard; W L Flejter; J Zackowski; F Tsien; S Schwartz
Journal:  Am J Hum Genet       Date:  1994-05       Impact factor: 11.025

7.  Efficient identification of marker chromosomes in 27 patients by stepwise hybridization with alpha-satellite DNA probes.

Authors:  R Plattner; N A Heerema; Y B Yurov; C G Palmer
Journal:  Hum Genet       Date:  1993-03       Impact factor: 4.132

8.  The origin of cytologically unidentifiable chromosome abnormalities: six cases ascertained by targeted chromosome-band painting.

Authors:  T Ohta; T Tohma; H Soejima; Y Fukushima; T Nagai; K Yoshiura; Y Jinno; N Niikawa
Journal:  Hum Genet       Date:  1993-08       Impact factor: 4.132

  8 in total

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