Literature DB >> 76322

High-resolution chromosome analysis in clinical medicine.

J J Yunis, M E Chandler.   

Abstract

The field of human cytogenetics has expanded considerably in the past few years due, to a large extent, to the application of the metaphase banding techniques. Among many advances, the chromosomal abnormalities involved in over thirty newly discovered syndromes have been defined and consistent chromosome defects have been observed in several neoplasias. Very recent improvements in culture techniques through cell synchronization and in chromosome treatments, such as the use of minimal exposure to colcemid and/or the use of agents that inhibit chromosome condensation, allow for the routine utilization of highly elongated and finely banded prophase chromosomes. These new techniques are being used clinically to uncover previously undetectable chromosome defects, to localize the exact break points involved in numerous duplication-deficiencies known in man, and to establish possible phenotype-genotype relationships at a refined level.

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Year:  1978        PMID: 76322

Source DB:  PubMed          Journal:  Prog Clin Pathol        ISSN: 0079-6174


  30 in total

1.  About classical molecular genetics, cytogenetic and molecular cytogenetic data not considered by Genome Reference Consortium and thus not included in genome browsers like UCSC, Ensembl or NCBI.

Authors:  Thomas Liehr
Journal:  Mol Cytogenet       Date:  2021-03-20       Impact factor: 2.009

Review 2.  Patterns of Chromosomal Aberrations in Solid Tumors.

Authors:  Marian Grade; Michael J Difilippantonio; Jordi Camps
Journal:  Recent Results Cancer Res       Date:  2015

3.  Malignant transformation of human fibroblasts caused by expression of a transfected T24 HRAS oncogene.

Authors:  P J Hurlin; V M Maher; J J McCormick
Journal:  Proc Natl Acad Sci U S A       Date:  1989-01       Impact factor: 11.205

4.  The impact of imprinting: Prader-Willi syndrome resulting from chromosome translocation, recombination, and nondisjunction.

Authors:  S Toth-Fejel; S Olson; K Gunter; F Quan; J Wolford; B W Popovich; R E Magenis
Journal:  Am J Hum Genet       Date:  1996-05       Impact factor: 11.025

5.  A non-centromeric C band variant on chromosome 11q23.2.

Authors:  D K Spak; K Johnston; T A Donlon
Journal:  J Med Genet       Date:  1989-08       Impact factor: 6.318

6.  Molecular cytogenetic evidence for amplification of chromosome-specific alphoid sequences at enlarged C-bands on chromosome 6.

Authors:  E W Jabs; N Carpenter
Journal:  Am J Hum Genet       Date:  1988-07       Impact factor: 11.025

7.  Characterization and organization of DNA sequences adjacent to the human telomere associated repeat (TTAGGG)n.

Authors:  B Weber; C Collins; C Robbins; R E Magenis; A D Delaney; J W Gray; M R Hayden
Journal:  Nucleic Acids Res       Date:  1990-06-11       Impact factor: 16.971

8.  Down syndrome phenotypes: the consequences of chromosomal imbalance.

Authors:  J R Korenberg; X N Chen; R Schipper; Z Sun; R Gonsky; S Gerwehr; N Carpenter; C Daumer; P Dignan; C Disteche
Journal:  Proc Natl Acad Sci U S A       Date:  1994-05-24       Impact factor: 11.205

9.  A simple method for high resolution banding of chromosomes in amniotic fluid cells.

Authors:  P Jäger; C Kuhn-Schlage
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

10.  The utility of chromosomal microarray analysis in developmental and behavioral pediatrics.

Authors:  Arthur L Beaudet
Journal:  Child Dev       Date:  2013-01-11
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