Oncologic surveillance for subjects with biallelic mismatch repair gene mutations: 10 year follow-up of a kindred. (Q48768831)

15 February 2018

title

Oncologic surveillance for subjects with biallelic mismatch repair gene mutations: 10 year follow-up of a kindred. (English)

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Steven Gallinger

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object named as

Steven Gallinger

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author name string

Carol A Durno

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Melyssa Aronson

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David Malkin

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Helen S L Chan

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publication date

16 December 2011

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published in

Pediatric Blood Cancer

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volume

59

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issue

4

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page(s)

652-656

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Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome.

cites work

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Hereditary and familial colon cancer

21 January 2018

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Constitutive deficiency in DNA mismatch repair

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The gastrointestinal phenotype of germline biallelic mismatch repair gene mutations

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Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: a prospective observational study

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

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

21 January 2018

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

21 January 2018

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

21 January 2018

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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

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Biallelic PMS2 mutations and a distinctive childhood cancer syndrome

21 January 2018

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

21 January 2018

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Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer

21 January 2018

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

21 January 2018

1 reference

Hepatic Adenomas Caused by Somatic HNF1A Mutations in Children With Biallelic Mismatch Repair Gene Mutations

21 January 2018

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21 January 2018

Identifiers

DOI

10.1002/PBC.24019

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15 February 2018

PubMed ID

22180144

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15 February 2018