Medulloblastoma, acute myelocytic leukemia and colonic carcinomas in a child with biallelic MSH6 mutations. (Q55468550)

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scientific article published in February 2007

Language	Label	Description	Also known as
English	Medulloblastoma, acute myelocytic leukemia and colonic carcinomas in a child with biallelic MSH6 mutations.	scientific article published in February 2007

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

12 July 2018

http://europepmc.org/abstract/MED/17259933

Medulloblastoma, acute myelocytic leukemia and colonic carcinomas in a child with biallelic MSH6 mutations. (English)

1 reference

Europe PubMed Central

PubMed publication ID

12 July 2018

http://europepmc.org/abstract/MED/17259933

medulloblastoma

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6

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Europe PubMed Central

PubMed publication ID

12 July 2018

http://europepmc.org/abstract/MED/17259933

Kathryn Pritchard-Jones

object named as

Kathryn Pritchard-Jones

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author name string

Richard H Scott

1

1 reference

Europe PubMed Central

PubMed publication ID

12 July 2018

http://europepmc.org/abstract/MED/17259933

Sahar Mansour

2

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Europe PubMed Central

PubMed publication ID

12 July 2018

http://europepmc.org/abstract/MED/17259933

Devinder Kumar

4

1 reference

Europe PubMed Central

PubMed publication ID

12 July 2018

http://europepmc.org/abstract/MED/17259933

Fergus MacSweeney

5

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Europe PubMed Central

PubMed publication ID

12 July 2018

http://europepmc.org/abstract/MED/17259933

publication date

1 February 2007

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Europe PubMed Central

PubMed publication ID

12 July 2018

http://europepmc.org/abstract/MED/17259933

Nature Clinical Practice Oncology

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Europe PubMed Central

PubMed publication ID

12 July 2018

http://europepmc.org/abstract/MED/17259933

4

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Europe PubMed Central

PubMed publication ID

12 July 2018

http://europepmc.org/abstract/MED/17259933

2

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Europe PubMed Central

PubMed publication ID

12 July 2018

http://europepmc.org/abstract/MED/17259933

130-134

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Europe PubMed Central

PubMed publication ID

12 July 2018

http://europepmc.org/abstract/MED/17259933

A homozygous MSH6 mutation in a child with café-au-lait spots, oligodendroglioma and rectal cancer

1 reference

https://api.crossref.org/works/10.1038%2FNCPONC0719

7 January 2021

based on heuristic

inferred from DOI database lookup

A homozygous mutation in MSH6 causes Turcot syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNCPONC0719

7 January 2021

based on heuristic

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Neurofibromatosis von Recklinghausen type I phenotype and early onset of cancers in siblings compound heterozygous for mutations in MSH6

1 reference

https://api.crossref.org/works/10.1038%2FNCPONC0719

7 January 2021

based on heuristic

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Compound heterozygosity for two MSH6 mutations in a patient with early onset of HNPCC-associated cancers, but without hematological malignancy and brain tumor

1 reference

https://api.crossref.org/works/10.1038%2FNCPONC0719

7 January 2021

based on heuristic

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Lower incidence of colorectal cancer and later age of disease onset in 27 families with pathogenic MSH6 germline mutations compared with families with MLH1 or MSH2 mutations: the German Hereditary Nonpolyposis Colorectal Cancer Consortium

1 reference

https://api.crossref.org/works/10.1038%2FNCPONC0719

7 January 2021

based on heuristic

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Use of the national institutes of health criteria for diagnosis of neurofibromatosis 1 in children.

1 reference

https://api.crossref.org/works/10.1038%2FNCPONC0719

7 January 2021

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inferred from DOI database lookup

The molecular basis of Turcot's syndrome

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https://api.crossref.org/works/10.1038%2FNCPONC0719

7 January 2021

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inferred from DOI database lookup

Biallelic BRCA2 mutations are associated with multiple malignancies in childhood including familial Wilms tumour

1 reference

https://api.crossref.org/works/10.1038%2FNCPONC0719

7 January 2021

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Medulloblastoma with adverse reaction to radiation therapy in nijmegen breakage syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNCPONC0719

7 January 2021

based on heuristic

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Bloom's syndrome. XX. The first 100 cancers

1 reference

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7 January 2021

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Colorectal cancer screening. Clinical practice guidelines in oncology

1 reference

https://api.crossref.org/works/10.1038%2FNCPONC0719

7 January 2021

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inferred from DOI database lookup

Mechanisms of therapy-related carcinogenesis

1 reference

https://api.crossref.org/works/10.1038%2FNCPONC0719

7 January 2021

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inferred from DOI database lookup

A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapy

1 reference

https://api.crossref.org/works/10.1038%2FNCPONC0719

7 January 2021

based on heuristic

inferred from DOI database lookup

Enrichment for DNA mismatch repair-deficient cells during treatment with cisplatin

1 reference

https://api.crossref.org/works/10.1038%2FNCPONC0719

7 January 2021

based on heuristic

inferred from DOI database lookup

Defective DNA mismatch repair in acute myeloid leukemia/myelodysplastic syndrome after organ transplantation

1 reference

https://api.crossref.org/works/10.1038%2FNCPONC0719

7 January 2021

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Mismatch repair status in the prediction of benefit from adjuvant fluorouracil chemotherapy in colorectal cancer

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/NCPONC0719

1 reference

Europe PubMed Central

PubMed publication ID

12 July 2018

http://europepmc.org/abstract/MED/17259933

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

12 July 2018

http://europepmc.org/abstract/MED/17259933

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