(Q35634119)

9 August 2017

title

Familial myelodysplastic syndromes, monosomy 7/trisomy 8, and mutator effects (English)

1 reference

9 August 2017

Franco Locatelli

1 reference

9 August 2017

Emanuela Maserati

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9 August 2017

Antonella Minelli

1 reference

9 August 2017

Giuseppe Menna

1 reference

9 August 2017

Maria Paola Cecchini

1 reference

9 August 2017

Maria Ester Bernardo

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9 August 2017

Gabriele Rossi

1 reference

9 August 2017

Paola De Filippi

1 reference

9 August 2017

Francesco Lo Curto

1 reference

9 August 2017

Cesare Danesino

1 reference

9 August 2017

Francesco Pasquali

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9 August 2017

publication date

1 January 2004

1 reference

Cancer Genetics and Cytogenetics

9 August 2017

published in

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9 August 2017

volume

148

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9 August 2017

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9 August 2017

page(s)

155-158

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Myelodysplastic syndromes in childhood--classification, epidemiology, and treatment

9 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900271-1

7 January 2021

Forty-four cases of childhood myelodysplasia with cytogenetics, documented by the Groupe Français de Cytogénétique Hématologique

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900271-1

7 January 2021

Familial acute myeloid leukaemia: four male members of a single family over three consecutive generations exhibiting anticipation

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900271-1

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%2803%2900271-1

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%2803%2900271-1

7 January 2021

Familial myelodysplastic syndrome with early age of onset

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900271-1

7 January 2021

Familial partial monosomy 7 and myelodysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900271-1

7 January 2021

Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900271-1

7 January 2021

Haematological abnormalities in Shwachman-Diamond syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900271-1

7 January 2021

Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900271-1

7 January 2021

New mechanisms of AML1 gene alteration in hematological malignancies

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2803%2900271-1

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%2803%2900271-1

7 January 2021

10.1016/S0165-4608(03)00271-1

Identifiers

DOI

1 reference

release_7ip7x3jmhjdyha53hthohhbqdi

9 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/7ip7x3jmhjdyha53hthohhbqdi

24 November 2022

mapped directly with Wikidata item

1 reference