(Q48003443)

7 February 2018

review article

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title

Cancer genetics in the new era of molecular biology. (English)

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7 February 2018

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H T Lynch

1

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7 February 2018

R M Fusaro

series ordinal

2

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7 February 2018

J F Lynch

series ordinal

3

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7 February 2018

language of work or name

English

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publication date

1 December 1997

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7 February 2018

Annals of the New York Academy of Sciences

published in

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7 February 2018

volume

833

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7 February 2018

page(s)

1-28

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7 February 2018

Hereditary nonpolyposis colorectal cancer (Lynch syndrome). An updated review

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1997.TB48588.X

Lessons from hereditary colorectal cancer

21 January 2018

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Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis.

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1749-6632.1997.TB48588.X

Linkage of early-onset familial breast cancer to chromosome 17q21

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1749-6632.1997.TB48588.X

Identification of the breast cancer susceptibility gene BRCA2

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1749-6632.1997.TB48588.X

Risks of cancer in BRCA1-mutation carriers. Breast Cancer Linkage Consortium

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1749-6632.1997.TB48588.X

A descriptive study of BRCA1 testing and reactions to disclosure of test results

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1749-6632.1997.TB48588.X

Prolonged survival as a component of a hereditary breast and nonpolyposis colon cancer

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1749-6632.1997.TB48588.X

Natural history of hereditary cancer of the breast and colon

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1997.TB48588.X

A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1997.TB48588.X

Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1749-6632.1997.TB48588.X

Loss of the normal NF1 allele from the bone marrow of children with type 1 neurofibromatosis and malignant myeloid disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1997.TB48588.X

A single ataxia telangiectasia gene with a product similar to PI-3 kinase

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1749-6632.1997.TB48588.X

Mutations associated with familial melanoma impair p16INK4 function.

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1749-6632.1997.TB48588.X

Tumour-derived p16 alleles encoding proteins defective in cell-cycle inhibition

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1749-6632.1997.TB48588.X

Familial atypical multiple mole melanoma (FAMMM) syndrome: genetic heterogeneity and malignant melanoma

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1749-6632.1997.TB48588.X

Tumour spectrum in the FAMMM syndrome

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1749-6632.1997.TB48588.X

Systemic cancer and the FAMMM syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1997.TB48588.X

Brief report: a familial syndrome of pancreatic cancer and melanoma with a mutation in the CDKN2 tumor-suppressor gene

21 January 2018

1 reference

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Hereditary nonpolyposis colorectal cancer: the syndrome, the genes, and historical perspectives.

21 January 2018

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Variable gastrointestinal and urologic cancers in a Lynch syndrome II kindred.

21 January 2018

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Better survival rates in patients with MLH1-associated hereditary colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1997.TB48588.X

Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype–phenotype correlation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1997.TB48588.X

Localization of the gene for Cowden disease to chromosome 10q22–23

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1997.TB48588.X

Increased Risk of Pancreatic Cancer in Melanoma-Prone Kindreds withp16INK4Mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1997.TB48588.X

The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1997.TB48588.X

10.1111/J.1749-6632.1997.TB48588.X

21 January 2018

Identifiers

DOI

1 reference

7 February 2018

release_nwxrceilnvbgjijafvvgtzznpm

Fatcat ID

0 references

PubMed ID

9616736

1 reference

7 February 2018