(Q57568035)

3

object named as

Jukka-Pekka Mecklin

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Heikki Järvinen

4

object named as

Heikki Järvinen

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Albert de la Chapelle

7

object named as

Albert de la Chapelle

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author name string

Päivi Peltomäki

2

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Reijo Salovaara

5

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Minna Nyström-Lahti

6

0 references

Lauri A. Aaltonen

https://scigraph.springernature.com/pub.10.1038/ng1294-405

8

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language of work or name

English

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publication date

December 1994

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published in

Nature Genetics

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volume

8

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page(s)

405-410

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issue

4

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exact match

0 references

cites work

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The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer

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Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

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Mutation of a mutL homolog in hereditary colon cancer

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Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer.

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Mutations of two PMS homologues in hereditary nonpolyposis colon cancer

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Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: an updated review

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Genetic mapping of a locus predisposing to human colorectal cancer

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Genetic mapping of a second locus predisposing to hereditary non–polyposis colon cancer

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Hypermutability and mismatch repair deficiency in RER+ tumor cells

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Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis

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Microsatellite instability in cancer of the proximal colon

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Close linkage to chromosome 3p and conservation of ancestral founding haplotype in hereditary nonpolyposis colorectal cancer families

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Cancer family syndrome. Genetic analysis of 22 Finnish kindreds

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Frequency of hereditary colorectal carcinoma

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PCR-based RFLP analysis allows genotyping of the short arm of chromosome 3 in small biopsies from patients with lung cancer

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All in the (cancer) family

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Diploid predominance in hereditary nonpolyposis colorectal carcinoma evaluated by flow cytometry

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Mutation and cancer: statistical study of retinoblastoma

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