Higher occurrence of childhood cancer in families with germline mutations in BRCA2, MMR and CDKN2A genes (Q81280342)

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7 January 2020

title

Higher occurrence of childhood cancer in families with germline mutations in BRCA2, MMR and CDKN2A genes (English)

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7 January 2020

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4

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7 January 2020

Håkan Olsson

6

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7 January 2020

author name string

Susanne Magnusson

1

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7 January 2020

Ake Borg

2

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7 January 2020

Ulf Kristoffersson

3

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7 January 2020

Thomas Wiebe

5

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7 January 2020

publication date

15 May 2008

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7 January 2020

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7 January 2020

volume

7

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7 January 2020

issue

4

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7 January 2020

page(s)

331-337

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

7 January 2020

cites work

1 reference

12 December 2020

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

1 reference

12 December 2020

Occupational exposures and non-Hodgkin's lymphoma in Southern Sweden

1 reference

12 December 2020

Homozygous germline mutation of CDKN2A/p16 and glucose-6-phosphate dehydrogenase deficiency in a multiple melanoma case

1 reference

12 December 2020

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

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12 December 2020

Mouse models of BRCA1 and BRCA2 deficiency: past lessons, current understanding and future prospects

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12 December 2020

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

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12 December 2020

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

1 reference

12 December 2020

PMS2 mutations in childhood cancer

1 reference

12 December 2020

Extensive somatic microsatellite mutations in normal human tissue.

1 reference

12 December 2020

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

1 reference

12 December 2020

Childhood cancer in families with and without BRCA1 or BRCA2 mutations ascertained at a high-risk breast cancer clinic

1 reference

12 December 2020

Human MLH1 deficiency predisposes to hematological malignancy and neurofibromatosis type 1

1 reference

12 December 2020

Review of alterations of the cyclin-dependent kinase inhibitor INK4 family genes p15, p16, p18 and p19 in human leukemia-lymphoma cells

1 reference

12 December 2020

A homozygous germ-line mutation in the human MSH2 gene predisposes to hematological malignancy and multiple café-au-lait spots

1 reference

12 December 2020

Shared genetic susceptibility to breast cancer, brain tumors, and Fanconi anemia

1 reference

12 December 2020

Biallelic inactivation of BRCA2 in Fanconi anemia

1 reference

12 December 2020

Early onset brain tumor and lymphoma in MSH2-deficient children

1 reference

12 December 2020

Neurofibromatosis and early onset of cancers in hMLH1-deficient children

1 reference

12 December 2020

Biallelic germline mutations of mismatch-repair genes: a possible cause for multiple pediatric malignancies

1 reference

12 December 2020

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

1 reference

12 December 2020

An estimate of the heritable fraction of childhood cancer

1 reference

12 December 2020

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

1 reference

12 December 2020

Increased risk of cancer among siblings of long-term childhood cancer survivors: a report from the childhood cancer survivor study.

1 reference

12 December 2020

Novel PMS2 pseudogenes can conceal recessive mutations causing a distinctive childhood cancer syndrome

1 reference

12 December 2020

A novelMSH2 germline mutation in homozygous state in two brothers with colorectal cancers diagnosed at the age of 11 and 12 years

1 reference

12 December 2020

Parental cancer in an unselected cohort of children with cancer referred to a single centre

1 reference

12 December 2020

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

1 reference

12 December 2020

Constitutive deficiency in DNA mismatch repair

1 reference

12 December 2020

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

1 reference

12 December 2020

A homozygous mutation in MSH6 causes Turcot syndrome

1 reference

12 December 2020