(Q78483042)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12419582%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

title

A new nonrandom unbalanced t(17;20) in myeloid malignancies (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12419582%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

author name string

Crisoula Patsouris

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12419582%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

Patricia M Michael

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12419582%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

Lynda J Campbell

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12419582%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

publication date

1 October 2002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12419582%20AND%20SRC:MED&resulttype=core&format=json

Cancer Genetics and Cytogenetics

14 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12419582%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

volume

138

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12419582%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12419582%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

page(s)

32-37

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12419582%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900579-4

7 January 2021

Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900579-4

7 January 2021

Identification of candidate genes on chromosome band 20q12 by physical mapping of translocation breakpoints found in myeloid leukemia cell lines

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900579-4

7 January 2021

Spectral karyotyping (SKY) refinement of a complex karyotype with t(20;21) in a Ph-positive CML patient submitted to peripheral blood stem cell transplantation.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900579-4

7 January 2021

Identification of two new translocations that disrupt the AML1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900579-4

7 January 2021

17p- syndrome arising from a novel dicentric translocation in a patient with acute myeloid leukemia

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900579-4

7 January 2021

dic(9;20): a new recurrent chromosome abnormality in adult acute lymphoblastic leukemia

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900579-4

7 January 2021

Monosomy 20 as a pointer to dicentric (9;20) in acute lymphoblastic leukemia

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900579-4

7 January 2021

De novo myelodysplastic syndrome (MDS) with deletion of the long arm of chromosome 20: a subtype of MDS with distinct hematological and prognostic features?

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900579-4

7 January 2021

Blast crisis of Ph-positive chronic myeloid leukemia with isochromosome 17q: report of 12 cases and review of the literature

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900579-4

7 January 2021

Association of 17p loss with late-stage or refractory disease in hematologic malignancy.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900579-4

7 January 2021

dic(5;17): a recurring abnormality in malignant myeloid disorders associated with mutations of TP53

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900579-4

7 January 2021

The 17p-syndrome: a distinct myelodysplastic syndrome entity?

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900579-4

7 January 2021

Mutations with loss of heterozygosity of p53 are common in therapy-related myelodysplasia and acute myeloid leukemia after exposure to alkylating agents and significantly associated with deletion or loss of 5q, a complex karyotype, and a poor progno

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900579-4

7 January 2021

Granulocyte maturation and the chromosome deletion 17p- in primary myelodysplastic syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900579-4

7 January 2021

10.1016/S0165-4608(02)00579-4

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12419582%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

1 reference