Isochromosome (7)(q10) in Shwachman Syndrome Without MDS/AML and Role of Chromosome 7 Anomalies in Myeloproliferative Disorders (Q61196691)

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1 November 2019

title

Isochromosome (7)(q10) in Shwachman syndrome without MDS/AML and role of chromosome 7 anomalies in myeloproliferative disorders (English)

1 reference

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myeloproliferative disorders

1 November 2019

main subject

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3

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1 November 2019

author name string

E Maserati

1

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1 November 2019

A Minelli

2

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1 November 2019

L Bonvini

4

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1 November 2019

A Marchi

5

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1 November 2019

M Bozzola

6

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1 November 2019

C Danesino

7

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1 November 2019

S Scappaticci

8

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1 November 2019

F Pasquali

9

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1 November 2019

publication date

1 September 2000

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Cancer Genetics and Cytogenetics

1 November 2019

published in

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1 November 2019

volume

121

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1 November 2019

issue

2

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1 November 2019

page(s)

167-171

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Shwachman syndrome: exocrine pancreatic dysfunction and variable phenotypic expression

1 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900246-6

7 January 2021

Haematological abnormalities in Shwachman-Diamond syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900246-6

7 January 2021

Malignant myeloid transformation with isochromosome 7q in Shwachman-Diamond syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900246-6

7 January 2021

Response to long-term hGH therapy in two children with Schwachman-Diamond syndrome associated with GH deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900246-6

7 January 2021

Shwachman syndrome and chromosome breakage

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900246-6

7 January 2021

Shwachman syndrome associated with de novo reciprocal translocation t(6;12)(q16.2;q21.2).

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900246-6

7 January 2021

Cloning of translocation breakpoints associated with Shwachman syndrome and identification of a candidate gene

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900246-6

7 January 2021

Exclusion of linkage of Shwachman-Diamond syndrome to chromosome regions 6q and 12q implicated by a de novo translocation

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900246-6

7 January 2021

A case of Shwachman syndrome with increased spontaneous chromosome breakage

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900246-6

7 January 2021

Is Shwachman syndrome (McKusick 26040) a chromosome breakage syndrome?

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900246-6

7 January 2021

Increased spontaneous chromosomal breakage in Shwachman syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900246-6

7 January 2021

Isochromosomes in neoplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900246-6

7 January 2021

Isochromosomes 7q and 17q in Wilms tumor

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900246-6

7 January 2021

Consistent presence of isochromosome 7q in hepatosplenic T gamma/delta lymphoma: a new cytogenetic-clinicopathologic entity

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900246-6

7 January 2021

Cytogenetic abnormalities in natural killer cell lymphoma/leukaemia--is there a consistent pattern?

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900246-6

7 January 2021

Constitutional trisomy 8 as first mutation in multistep carcinogenesis: clinical, cytogenetic, and molecular data on three cases

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900246-6

7 January 2021

Genetic alterations in leukemias and lymphomas: impressive progress and continuing complexity

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900246-6

7 January 2021

Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900246-6

7 January 2021

Human PEG1/MEST, an imprinted gene on chromosome 7

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2800%2900246-6

7 January 2021

10.1016/S0165-4608(00)00246-6

Identifiers

DOI

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1 November 2019

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