Literature DB >> 975933

Comparison of G-, Q-, and R-banding in 28 cases of chromosomal abnormalities.

R S Verma, D C Peakman, A Robinson, H A Lubs.   

Abstract

Twenty-eight cases of chromosomal abnormalities were ascertained using G-banding. Seventeen of these had structural abnormalities of a complex nature and are discussed in detail. An independent assessment of chromosome abnormalities was carried out using sequential Q- and R-banding. In no case was there a difference in the identification of the abnormal chromosome, but in two cases a more precise localization or definition of the abnormality was obtained from the R-banded cells. In one case the initial diagnosis of the terminal deletion was altered to interstitial deletion; in the second case a break point in one chromosome involved in a reciprocal translocation was found to be in a different band by R-banding. In several others better delineation of break points or confirmation of complex abnormalities was obtained from the R-banded cells. R-banding was especially helpful in the localization of break points because of the color differentiation obtained with acridine orange. Q-banding was not found to have added any additional information. It was concluded from this study that the use of both G-banding and R-banding in complex abnormalities proved worthwhile.

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Year:  1976        PMID: 975933     DOI: 10.1159/000130665

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN: 0301-0171


  3 in total

1.  De novo inv(17)(p11.2q21.3) in an intellectually disabled girl: appraisal of 21 inv(17) constitutional instances.

Authors:  Miriam Partida-Pérez; María G Domínguez; Vivian Alejandra Neira; Luis E Figuera; Horacio Rivera
Journal:  J Genet       Date:  2012-08       Impact factor: 1.166

2.  Precise identification of human chromosomal abnormalities.

Authors:  R S Verma; H Dosik
Journal:  Am J Hum Genet       Date:  1979-01       Impact factor: 11.025

Review 3.  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

  3 in total

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