(Q51129460)

English

Clinical genetics & human genome variation: the 2008 Human Genome Variation Society scientific meeting.

scientific article published in May 2009

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scholarly article

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Europe PubMed Central

PubMed publication ID

19260058

retrieved

30 March 2018

reference URL

http://europepmc.org/abstract/MED/19260058

title

Clinical genetics & human genome variation: the 2008 Human Genome Variation Society scientific meeting. (English)

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stated in

Europe PubMed Central

PubMed publication ID

19260058

retrieved

30 March 2018

reference URL

http://europepmc.org/abstract/MED/19260058

author name string

William S Oetting

series ordinal

1

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Europe PubMed Central

PubMed publication ID

19260058

retrieved

30 March 2018

reference URL

http://europepmc.org/abstract/MED/19260058

publication date

1 May 2009

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Europe PubMed Central

PubMed publication ID

19260058

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30 March 2018

reference URL

http://europepmc.org/abstract/MED/19260058

published in

Human Mutation

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Europe PubMed Central

PubMed publication ID

19260058

retrieved

30 March 2018

reference URL

http://europepmc.org/abstract/MED/19260058

volume

30

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Europe PubMed Central

PubMed publication ID

19260058

retrieved

30 March 2018

reference URL

http://europepmc.org/abstract/MED/19260058

issue

5

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Europe PubMed Central

PubMed publication ID

19260058

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30 March 2018

reference URL

http://europepmc.org/abstract/MED/19260058

page(s)

852-856

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Europe PubMed Central

PubMed publication ID

19260058

retrieved

30 March 2018

reference URL

http://europepmc.org/abstract/MED/19260058

cites work

Genetic evidence and integration of various data sources for classifying uncertain variants into a single model

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1002%2FHUMU.20987

retrieved

7 January 2021

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Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results

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Crossref

reference URL

https://api.crossref.org/works/10.1002%2FHUMU.20987

retrieved

7 January 2021

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ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FHUMU.20987

retrieved

7 January 2021

based on heuristic

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Assessing pathogenicity: overview of results from the IARC Unclassified Genetic Variants Working Group

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FHUMU.20987

retrieved

7 January 2021

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Identifiers

DOI

10.1002/HUMU.20987

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19260058

retrieved

30 March 2018

reference URL

http://europepmc.org/abstract/MED/19260058

PubMed publication ID

19260058

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19260058

retrieved

30 March 2018

reference URL

http://europepmc.org/abstract/MED/19260058

ResearchGate publication ID

24176156

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(Q51129460)

Clinical genetics & human genome variation: the 2008 Human Genome Variation Society scientific meeting.

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