Literature DB >> 1494546

Analysis of chromosome 21 copy number in uncultured amniocytes by fluorescence in situ hybridization using a cosmid contig.

Y L Zheng1, M A Ferguson-Smith, J P Warner, M E Ferguson-Smith, C A Sargent, N P Carter.   

Abstract

A comparison of the use of chromosome 21-specific libraries, DOP-PCR 21 paints, yeast artificial chromosome (YAC) clones, single cosmids, and a 21q cosmid contig as probes for the detection of the copy number of chromosome 21 in interphase cells by fluorescence in situ hybridization shows that the cosmid contig is a satisfactory probe for interphase analysis of chromosome 21. The contig cCMP21.a, which is 55 kb in length, is highly chromosome 21-specific and produces intense, compact signals in a high proportion of interphase cells. A retrospective blind analysis of coded uncultured amniotic fluid samples correctly detected four trisomy 21 cases out of 49 samples.

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Year:  1992        PMID: 1494546     DOI: 10.1002/pd.1970121113

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  11 in total

1.  Preimplantation genetic diagnosis for couples at high risk of Down syndrome pregnancy owing to parental translocation or mosaicism.

Authors:  C M Conn; J Cozzi; J C Harper; R M Winston; J D Delhanty
Journal:  J Med Genet       Date:  1999-01       Impact factor: 6.318

2.  Combined immunocytogenetic and molecular cytogenetic analysis of meiosis I human spermatocytes.

Authors:  A L Barlow; M A Hultén
Journal:  Chromosome Res       Date:  1996-12       Impact factor: 5.239

3.  A fast, novel approach for DNA fibre-fluorescence in situ hybridization analysis.

Authors:  S M Mann; D J Burkin; D K Grin; M A Ferguson-Smith
Journal:  Chromosome Res       Date:  1997-04       Impact factor: 5.239

4.  The critical region of overlap defining the AZFa male infertility interval of proximal Yq contains three transcribed sequences.

Authors:  C A Sargent; C A Boucher; S Kirsch; G Brown; B Weiss; A Trundley; P Burgoyne; N Saut; C Durand; N Levy; P Terriou; T Hargreave; H Cooke; M Mitchell; G A Rappold; N A Affara
Journal:  J Med Genet       Date:  1999-09       Impact factor: 6.318

5.  Rapid prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization: clinical experience with 4,500 specimens.

Authors:  B E Ward; S L Gersen; M P Carelli; N M McGuire; W R Dackowski; M Weinstein; C Sandlin; R Warren; K W Klinger
Journal:  Am J Hum Genet       Date:  1993-05       Impact factor: 11.025

6.  FISH detection of trisomy 21 in interphase by the simultaneous use of two differentially labelled cosmid contigs.

Authors:  A F Davies; L Barber; M Murer-Orlando; M Bobrow; M Adinolfi
Journal:  J Med Genet       Date:  1994-09       Impact factor: 6.318

7.  A rearrangement on chromosome 5 of an expressed human beta-glucuronidase pseudogene.

Authors:  C A Sargent; I J Chalmers; M Leversha; N A Affara
Journal:  Mamm Genome       Date:  1994-12       Impact factor: 2.957

Review 8.  Cell cycle activation and aneuploid neurons in Alzheimer's disease.

Authors:  Thomas Arendt
Journal:  Mol Neurobiol       Date:  2012-04-13       Impact factor: 5.590

9.  Prenatal diagnosis from maternal blood: simultaneous immunophenotyping and FISH of fetal nucleated erythrocytes isolated by negative magnetic cell sorting.

Authors:  Y L Zheng; N P Carter; C M Price; S M Colman; P J Milton; G A Hackett; M F Greaves; M A Ferguson-Smith
Journal:  J Med Genet       Date:  1993-12       Impact factor: 6.318

Review 10.  Neuronal aneuploidy in health and disease: a cytomic approach to understand the molecular individuality of neurons.

Authors:  Thomas Arendt; Birgit Mosch; Markus Morawski
Journal:  Int J Mol Sci       Date:  2009-04-15       Impact factor: 6.208

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