Penetrance of HNPCC-related cancers in a retrolective cohort of 12 large Newfoundland families carrying a MSH2 founder mutation: an evaluation using modified segregation models. - Wikidata - awgldk - TriplyDB

Penetrance of HNPCC-related cancers in a retrolective cohort of 12 large Newfoundland families carrying a MSH2 founder mutation: an evaluation using modified segregation models.

Penetrance of HNPCC-related cancers in a retrolective cohort of 12 large Newfoundland families carrying a MSH2 founder mutation: an evaluation using modified segregation models.

http://www.wikidata.org/entity/Q37417652

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Genetic testing for Lynch syndrome: family communication and motivation Impact of colonoscopic screening in male and female Lynch syndrome carriers with an MSH2 mutation.Cancer risks and immunohistochemical profiles linked to the Danish MLH1 Lynch syndrome founder mutation.

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P2860

Penetrance of HNPCC-related cancers in a retrolective cohort of 12 large Newfoundland families carrying a MSH2 founder mutation: an evaluation using modified segregation models.

http://www.wikidata.org/entity/Q37417652

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 28 October 2009

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Penetrance of HNPCC-related ca ...... g modified segregation models.

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Penetrance of HNPCC-related ca ...... g modified segregation models.

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Penetrance of HNPCC-related ca ...... g modified segregation models.

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Penetrance of HNPCC-related ca ...... g modified segregation models.

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Penetrance of HNPCC-related ca ...... g modified segregation models.

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Penetrance of HNPCC-related ca ...... g modified segregation models.

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Hereditary Cancer in Clinical Practice

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Penetrance of HNPCC-related ca ...... g modified segregation models.

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Elena Parkhomenko

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Jane Green

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John McLaughlin

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Karen A Kopciuk

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Laurent Briollais

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Patrick Parfrey

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Yun-Hee Choi

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Estimating penetrance from family data using a retrospective likelihood when ascertainment depends on genotype and age of onset.

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Conditioning on subsets of the data: applications to ascertainment and other genetic problems

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