Unclassified variants in disease-causing genes: nonuniformity of genetic testing and counselling, a proposal for guidelines

Geraldine R Vink; Christi J van Asperen; Peter Devilee; Martijn H Breuning; Egbert Bakker

doi:10.1038/sj.ejhg.5201379

Unclassified variants in disease-causing genes: nonuniformity of genetic testing and counselling, a proposal for guidelines

Geraldine R Vink^*
, Christi J van Asperen
, Peter Devilee
, Martijn H Breuning
, Egbert Bakker

^*Corresponding author for this work

Research output: Contribution to journal › Article › Academic › peer-review

Original language	English
Pages (from-to)	525-7
Number of pages	3
Journal	European Journal of Human Genetics
Volume	13
Issue number	5
DOIs	https://doi.org/10.1038/sj.ejhg.5201379
Publication status	Published - May 2005

Keywords

DNA, Neoplasm/analysis
Family Health
Female
Genes, BRCA1
Genes, BRCA2
Genetic Counseling/standards
Genetic Predisposition to Disease
Genetic Variation
Genetics, Medical/trends
Humans
Netherlands
Patient Education as Topic
Polymorphism, Genetic
Practice Guidelines as Topic

Access to Document

10.1038/sj.ejhg.5201379

Cite this

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title = "Unclassified variants in disease-causing genes: nonuniformity of genetic testing and counselling, a proposal for guidelines",

keywords = "DNA, Neoplasm/analysis, Family Health, Female, Genes, BRCA1, Genes, BRCA2, Genetic Counseling/standards, Genetic Predisposition to Disease, Genetic Variation, Genetics, Medical/trends, Humans, Netherlands, Patient Education as Topic, Polymorphism, Genetic, Practice Guidelines as Topic",

author = "Vink, \{Geraldine R\} and \{van Asperen\}, \{Christi J\} and Peter Devilee and Breuning, \{Martijn H\} and Egbert Bakker",

year = "2005",

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AU - van Asperen, Christi J

AU - Devilee, Peter

AU - Breuning, Martijn H

AU - Bakker, Egbert

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KW - Female

KW - Genes, BRCA1

KW - Genes, BRCA2

KW - Genetic Counseling/standards

KW - Genetic Predisposition to Disease

KW - Genetic Variation

KW - Genetics, Medical/trends

KW - Humans

KW - Netherlands

KW - Patient Education as Topic

KW - Polymorphism, Genetic

KW - Practice Guidelines as Topic

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DO - 10.1038/sj.ejhg.5201379

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SN - 1018-4813

VL - 13

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JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

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