(Q24644421)

English

FISH and SNP-A karyotyping in myelodysplastic syndromes: improving cytogenetic detection of del(5q), monosomy 7, del(7q), trisomy 8 and del(20q)

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scholarly article

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FISH and SNP-A karyotyping in myelodysplastic syndromes: improving cytogenetic detection of del(5q), monosomy 7, del(7q), trisomy 8 and del(20q) (English)

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Jaroslaw P. Maciejewski

10

object named as

Jaroslaw P Maciejewski

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author name string

Hideki Makishima

1

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Manjot Rataul

2

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Lukasz P Gondek

3

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Jungwon Huh

4

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James R Cook

5

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Karl S Theil

6

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Mikkael A Sekeres

7

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Elizabeth Kuczkowski

8

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Christine O'Keefe

9

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language of work or name

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publication date

April 2010

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Leukemia Research

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34

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4

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447-53

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Chromosomal lesions and uniparental disomy detected by SNP arrays in MDS, MDS/MPD, and MDS-derived AML

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826525

7 April 2017

International scoring system for evaluating prognosis in myelodysplastic syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826525

7 April 2017

Loss of heterozygosity 4q24 and TET2 mutations associated with myelodysplastic/myeloproliferative neoplasms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826525

27 September 2017

Whole genome scanning as a cytogenetic tool in hematologic malignancies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826525

27 September 2017

Clonality of the stem cell compartment during evolution of myelodysplastic syndromes and other bone marrow failure syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826525

27 September 2017

Chromosomal deletions in the myelodysplastic syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826525

27 September 2017

Molecular definition of chromosome arm 5q deletion end points and detection of hidden aberrations in patients with myelodysplastic syndromes and isolated del(5q) using oligonucleotide array CGH.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826525

28 November 2018

Detection and monitoring of trisomy 8 by fluorescence in situ hybridization in acute myeloid leukemia: a multicentric study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2826525

28 November 2018

High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration

1 reference

https://pubmed.ncbi.nlm.nih.gov/19758696

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fluorescence in situ hybridization: a sensitive method for trisomy 8 detection in bone marrow specimens

1 reference

https://pubmed.ncbi.nlm.nih.gov/19758696

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic analysis has strong independent prognostic value in de novo myelodysplastic syndromes and can be incorporated in a new scoring system: a report on 408 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/19758696

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fluorescence in situ hybridization improves the detection of monosomy 7 in myelodysplastic syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19758696

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.LEUKRES.2009.08.023

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