(Q35005783)

5 August 2017

title

Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells (English)

1 reference

5 August 2017

Roberto Valli

1

1 reference

5 August 2017

Cristina Marletta

2

1 reference

5 August 2017

Barbara Pressato

3

1 reference

5 August 2017

Giuseppe Montalbano

4

1 reference

5 August 2017

Francesco Lo Curto

5

1 reference

5 August 2017

Francesco Pasquali

6

1 reference

5 August 2017

Emanuela Maserati

7

1 reference

5 August 2017

publication date

9 May 2011

1 reference

5 August 2017

published in

Molecular Cytogenetics

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5 August 2017

volume

4

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5 August 2017

page(s)

13

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Evidence-based genomic diagnosis characterized chromosomal and cryptic imbalances in 30 elderly patients with myelodysplastic syndrome and acute myeloid leukemia

5 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3101650

Development of new postnatal diagnostic methods for chromosome disorders

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3101650

Assessing karyotype precision by microarray-based comparative genomic hybridization in the myelodysplastic/myeloproliferative syndromes

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3101650

Comparative analysis of copy number detection by whole-genome BAC and oligonucleotide array CGH

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3101650

Application of array-based whole genome scanning technologies as a cytogenetic tool in haematological malignancies

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3101650

Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3101650

Clinical utility of contemporary molecular cytogenetics

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3101650

Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patients.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3101650

Establishment and study of different real-time polymerase chain reaction assays for the quantification of cells with deletions of chromosome 7.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3101650

Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3101650

Detection of large-scale variation in the human genome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3101650

Multiple putative oncogenes at the chromosome 20q amplicon contribute to colorectal adenoma to carcinoma progression.

8 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8166-4-13

High-resolution whole genome tiling path array CGH analysis of CD34+ cells from patients with low-risk myelodysplastic syndromes reveals cryptic copy number alterations and predicts overall and leukemia-free survival.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8166-4-13

The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8166-4-13

Evaluating chromosomal mosaicism by array comparative genomic hybridization in hematological malignancies: the proposal of a formula

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3101650

Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics

26 October 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8166-4-13

Detection of low-level mosaicism by array CGH in routine diagnostic specimens

21 January 2018

1 reference

12 December 2020

Chromosomal changes characterize head and neck cancer with poor prognosis

1 reference

12 December 2020

Oligonucleotide array-CGH reveals cryptic gene copy number alterations in karyotypically normal acute myeloid leukemia

1 reference

12 December 2020

Shwachman syndrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies

1 reference

12 December 2020

Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR

1 reference

12 December 2020

Identifiers

DOI

10.1186/1755-8166-4-13

1 reference

Dimensions Publication ID

5 August 2017

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0 references

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5 August 2017

1 reference