(Q37763509)

22 August 2017

The gastrointestinal phenotype of germline biallelic mismatch repair gene mutations (English)

1 reference

22 August 2017

1 reference

1 reference

Philip M Sherman

3

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Steven Gallinger

series ordinal

4

object named as

Steven Gallinger

1 reference

22 August 2017

Carol A Durno

1

1 reference

PubMed ID

20531397

22 August 2017

Spring Holter

series ordinal

2

1 reference

PubMed ID

20531397

22 August 2017

language of work or name

English

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publication date

8 June 2010

1 reference

The American Journal of Gastroenterology

22 August 2017

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22 August 2017

105

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22 August 2017

11

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22 August 2017

2449-2456

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Family history and molecular features of children, adolescents, and young adults with colorectal carcinoma

22 August 2017

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

Genetic predisposition to colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

Constitutive deficiency in DNA mismatch repair

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

Syndrome of early onset colon cancers, hematologic malignancies & features of neurofibromatosis in HNPCC families with homozygous mismatch repair gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

Café-au-lait macules and pediatric malignancy caused by biallelic mutations in the DNA mismatch repair (MMR) gene PMS2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

The molecular basis of Turcot's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

Homozygous PMS2 deletion causes a severe colorectal cancer and multiple adenoma phenotype without extraintestinal cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

Two PMS2 mutations in a Turcot syndrome family with small bowel cancers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

Homozygous PMS2 germline mutations in two families with early-onset haematological malignancy, brain tumours, HNPCC-associated tumours, and signs of neurofibromatosis type 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

A homozygous mutation in MSH6 causes Turcot syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

Inherited susceptibility to common cancers

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

Genetic predisposition to colorectal cancer: new pieces in the pediatric puzzle

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

Turcot's syndrome: a diagnostic consideration in a child with primary adenocarcinoma of the colon

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

Colorectal cancer in two pre-teenage siblings with familial adenomatous polyposis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic review

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

Clinical impact of capsule endoscopy on management of gastrointestinal disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

Constitutive deficiency in DNA mismatch repair: is it time for Lynch III?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

Constitutional mismatch repair-deficiency syndrome: have we so far seen only the tip of an iceberg?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

Biallelic PMS2 mutations and a distinctive childhood cancer syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

Novel biallelic mutations in MSH6 and PMS2 genes: gene conversion as a likely cause of PMS2 gene inactivation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

Polyposis and early cancer in a patient with low penetrant mutations in MSH6 and APC: hereditary colorectal cancer as a polygenic trait.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

PMS2 mutations in childhood cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

Café-au-lait spots and early onset colorectal neoplasia: a variant of HNPCC?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

Rhabdomyosarcoma in patients with constitutional mismatch-repair-deficiency syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

Gastrointestinal cancers and neurofibromatosis type 1 features in children with a germline homozygous MLH1 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

Compound heterozygosity for twoMSH6 mutations in a patient with early onset colorectal cancer, vitiligo and systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJG.2010.215

21 January 2018

Identifiers

DOI

10.1038/AJG.2010.215

1 reference

22 August 2017

1 reference

PubMed ID

20531397