Screening of BMPR1a for pathogenic mutations in familial colorectal cancer type X families from Newfoundland.

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Hereditary Nonpolyposis Colorectal Cancer and Cancer Syndromes: Recent Basic and Clinical Discoveries.

P2860

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P2860

Screening of BMPR1a for pathogenic mutations in familial colorectal cancer type X families from Newfoundland.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

@zh-hans

2017年学术文章

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@yue

2017年學術文章

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name

Screening of BMPR1a for pathog ...... X families from Newfoundland.

@en

Screening of BMPR1a for pathog ...... X families from Newfoundland.

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type

Item

label

Screening of BMPR1a for pathog ...... X families from Newfoundland.

@en

Screening of BMPR1a for pathog ...... X families from Newfoundland.

@nl

prefLabel

Screening of BMPR1a for pathog ...... X families from Newfoundland.

@en

Screening of BMPR1a for pathog ...... X families from Newfoundland.

@nl

P1476

Screening of BMPR1a for pathog ...... X families from Newfoundland.

@en

P2093

Jane S Green

http://www.w3.org/2001/XMLSchema#string

Michael O Woods

http://www.w3.org/2001/XMLSchema#string

P2860

Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type X

Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial disease

Rare disruptive mutations and their contribution to the heritable risk of colorectal cancer.

Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer

A population-based study of hereditary non-polyposis colorectal cancer: evidence of pathologic and genetic heterogeneity.

Very high incidence of familial colorectal cancer in Newfoundland: a comparison with Ontario and 13 other population-based studies.

BMPR1A mutations in early-onset colorectal cancer with mismatch repair proficiency.

BMPR1A mutations in hereditary nonpolyposis colorectal cancer without mismatch repair deficiency.

P2888

s10689-017-0016-8

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205-208

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scholarly article

P356

10.1007/S10689-017-0016-8

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

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Daniel R Evans

P577

2017-06-28T00:00:00Z

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P698

28660566

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P921

colorectal cancer

Screening of BMPR1a for pathogenic mutations in familial colorectal cancer type X families from Newfoundland.

about

P2860

P2860

Screening of BMPR1a for pathogenic mutations in familial colorectal cancer type X families from Newfoundland.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P698

P921