(Q33479671)

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Improved interpretation of complex chromosomal rearrangements by combined GTG banding and in situ suppression hybridization using chromosome-specific libraries and cosmid probes

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scholarly article

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Europe PubMed Central

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27 July 2017

Improved interpretation of complex chromosomal rearrangements by combined GTG banding and in situ suppression hybridization using chromosome-specific libraries and cosmid probes (English)

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Europe PubMed Central

PubMed publication ID

27 July 2017

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Devilee P

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27 July 2017

author name string

Smit VT

1

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27 July 2017

Wessels JW

2

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27 July 2017

Mollevanger P

3

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27 July 2017

Dauwerse JG

4

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27 July 2017

van Vliet M

5

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27 July 2017

Beverstock GC

6

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27 July 2017

Breuning MH

7

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27 July 2017

Raap AK

9

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27 July 2017

Cornelisse CJ

10

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27 July 2017

publication date

1 July 1991

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27 July 2017

Genes, Chromosomes and Cancer

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27 July 2017

3

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27 July 2017

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27 July 2017

239-248

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27 July 2017

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Chromosome aberrations in metastatic ovarian cancer: relationship with abnormalities in primary tumors

1 reference

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Simultaneous localization of cosmids and chromosome R-banding by fluorescence microscopy: application to regional mapping of human chromosome 11.

1 reference

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Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes

1 reference

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Rapid interphase and metaphase assessment of specific chromosomal changes in neuroectodermal tumor cells by in situ hybridization with chemically modified DNA probes.

1 reference

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7 January 2021

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Rapid detection of chromosome 16 inversion in acute nonlymphocytic leukemia, subtype M4: regional localization of the breakpoint in 16p

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At least four different chromosomal regions are involved in loss of heterozygosity in human breast carcinoma

1 reference

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Mapping small DNA sequences by fluorescence in situ hybridization directly on banded metaphase chromosomes

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Structural evidence for the authenticity of the human retinoblastoma gene

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A simple technique for obtaining high quality chromosome preparations from chorionic villus samples using FdU synchronization

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In situ hybridization as a tool to study numerical chromosome aberrations in solid bladder tumors

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Direct nonradioactive in situ hybridization of somatic cell hybrid DNA to human lymphocyte chromosomes

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Progressive chromosome changes associated with different sites of one ovarian carcinoma

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Enzymatic synthesis of biotin-labeled polynucleotides: novel nucleic acid affinity probes

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Detection of chromosome aberrations in interphase tumor nuclei by nonradioactive in situ hybridization

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Multiple fluorescence in situ hybridization.

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Common marker chromosomes in ovarian cancer

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Consistent occurrence of a 19p+ marker chromosome and loss of 11p material in ovarian seropapillary cystadenocarcinomas

1 reference

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Cytogenetic analysis by in situ hybridization with fluorescently labeled nucleic acid probes

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Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.

1 reference

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Selective isolation of cosmid clones by homologous recombination in Escherichia coli

1 reference

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Cytogenetic analysis of four human ovarian carcinoma cell lines

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Combined GTG-banding and nonradioactive in situ hybridization improves characterization of complex karyotypes

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870030402

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Chromosome aberrations in nine patients with ovarian cancer

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7 January 2021

based on heuristic

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Identifiers

10.1002/GCC.2870030402

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

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