Literature DB >> 15162070

mBAND: a high resolution multicolor banding technique for the detection of complex intrachromosomal aberrations.

I Chudoba1, G Hickmann, T Friedrich, A Jauch, P Kozlowski, G Senger.   

Abstract

Precise breakpoint definition of chromosomal rearrangements using conventional banding techniques often fails, especially when more than two breakpoints are involved. The classic banding procedure results in a pattern of alternating light and dark bands. Hence, in banded chromosomes a specific chromosomal band is rather identified by the surrounding banding pattern than by its own specific morphology. In chromosomal rearrangements the original pattern is altered and therefore the unequivocal determination of breakpoints is not obvious. The multicolor banding technique (mBAND, see Chudoba et al., 1999) is able to identify breakpoints unambiguously, even in highly complex chromosomal aberrations. The mBAND technique is presented and illustrated in a case of intrachromosomal rearrangement with seven breakpoints all having occurred on one chromosome 16, emphasizing the unique analyzing power of mBAND as compared to conventional banding techniques. Copyright 2003 S. Karger AG, Basel

Mesh:

Year:  2004        PMID: 15162070     DOI: 10.1159/000077521

Source DB:  PubMed          Journal:  Cytogenet Genome Res        ISSN: 1424-8581            Impact factor:   1.636


  8 in total

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Journal:  Radiat Prot Dosimetry       Date:  2016-07-13       Impact factor: 0.972

4.  Rearrangements of the telomeric region of mouse chromosome 11 in Pre-B ABL/MYC cells revealed by mBANDing, spectral karyotyping, and fluorescence in-situ hybridization with a subtelomeric probe.

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Journal:  Chromosome Res       Date:  2004       Impact factor: 5.239

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6.  Multicolor banding remains an important adjunct to array CGH and conventional karyotyping.

Authors:  Susan M Bint; Angela F Davies; Caroline Mackie Ogilvie
Journal:  Mol Cytogenet       Date:  2013-12-05       Impact factor: 2.009

7.  Insulin-like growth factor type 1 deficiency in a Moroccan patient with de novo inverted duplication 9p24p12 and developmental delay: a case report.

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Journal:  J Med Case Rep       Date:  2016-05-13

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  8 in total

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