(Q61196689)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11172908%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

title

Familial partial monosomy 7 and myelodysplasia: different parental origin of the monosomy 7 suggests action of a mutator gene (English)

1 reference

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3 November 2019

4

1 reference

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3 November 2019

Carla Olivieri

5

1 reference

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3 November 2019

author name string

A Minelli

1

1 reference

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3 November 2019

E Maserati

2

1 reference

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3 November 2019

G Giudici

3

1 reference

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3 November 2019

L Bonvini

6

1 reference

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3 November 2019

P De Filippi

7

1 reference

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3 November 2019

A Biondi

8

1 reference

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3 November 2019

F Lo Curto

9

1 reference

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3 November 2019

F Pasquali

10

1 reference

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3 November 2019

C Danesino

11

1 reference

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3 November 2019

publication date

1 January 2001

1 reference

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Cancer Genetics and Cytogenetics

3 November 2019

published in

1 reference

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3 November 2019

volume

124

1 reference

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3 November 2019

issue

2

1 reference

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3 November 2019

page(s)

147-151

1 reference

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Ataxia-pancytopenia: syndrome of cerebellar ataxia, hypoplastic anemia, monosomy 7, and acute myelogenous leukemia

3 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900344-7

7 January 2021

Familial leukemia and aplastic anemia associated with monosomy 7

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900344-7

7 January 2021

Evidence implicating heterozygous deletion of chromosome 7 in the pathogenesis of familial leukemia associated with monosomy 7.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900344-7

7 January 2021

Myelodysplastic syndrome, juvenile myelomonocytic leukemia, and acute myeloid leukemia associated with complete or partial monosomy 7. European Working Group on MDS in Childhood (EWOG-MDS)

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900344-7

7 January 2021

Familial acute myeloid leukemia with monosomy 7: late onset and involvement of a multipotential progenitor cell

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900344-7

7 January 2021

Familial bone marrow monosomy 7. Evidence that the predisposing locus is not on the long arm of chromosome 7.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900344-7

7 January 2021

Complex structural involvement of chromosome 7 in primary myelodysplastic syndromes determined by fluorescence in situ hybridization

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900344-7

7 January 2021

Myelodysplastic syndrome with hypereosinophilia and a nonrandom chromosomal abnormality dic(1;7): confirmation of eosinophil clonal involvement by fluorescence in situ hybridization.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900344-7

7 January 2021

Refractory cytopenia with t(1;7),+8 abnormality and dysplastic eosinophils showing intranuclear Charcot-Leyden crystals: a fluorescence in situ hybridization study

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900344-7

7 January 2021

Ph-positive CML in blastic phase with monosomy 7 in a Down syndrome patient. Monitoring by interphase cytogenetics and demonstration of maternal allelic loss

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900344-7

7 January 2021

10.1016/S0165-4608(00)00344-7

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11172908%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference