(Q35084017)

6 August 2017

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title

Ethical issues raised by genetic testing with oligonucleotide microarrays (English)

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6 August 2017

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Wayne W Grody

1

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6 August 2017

1 February 2003

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6 August 2017

Molecular Biotechnology

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6 August 2017

23

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6 August 2017

2

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6 August 2017

127-138

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https://scigraph.springernature.com/pub.10.1385/mb:23:2:127

6 August 2017

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cites work

The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals

1 reference

12 December 2020

1 reference

12 December 2020

Genetic testing for susceptibility to adult-onset cancer. The process and content of informed consent

1 reference

12 December 2020

The Privacy Rule: HIPAA standards for the privacy of individually identifiable health information.

1 reference

12 December 2020

Pedigrees-publish? or perish the thought?

1 reference

12 December 2020

Bad for your health: are gene patents stopping patients getting the latest tests?

1 reference

12 December 2020

A model agreement for genetic research in socially identifiable populations

1 reference

12 December 2020

Statement of the American Society of Clinical Oncology: genetic testing for cancer susceptibility, Adopted on February 20, 1996

1 reference

12 December 2020

Group identity and human diversity: keeping biology straight from culture.

1 reference

12 December 2020

BRCA1 sequence analysis in women at high risk for susceptibility mutations. Risk factor analysis and implications for genetic testing.

1 reference

12 December 2020

Research and stored tissues. Persons as sources, samples as persons?

1 reference

12 December 2020

FDA regulation of analyte-specific reagents (ASRs). Implications for nucleic acid-based molecular testing

1 reference

12 December 2020

NBAC issues biosamples report

1 reference

12 December 2020

That lonesome grail: The Code of Codes: Scientific and Social Issues in the Human Genome Project

1 reference

12 December 2020

Predictive genetic testing: from basic research to clinical practice

1 reference

12 December 2020

Privacy and confidentiality in the publication of pedigrees: a survey of investigators and biomedical journals.

1 reference

12 December 2020

Informed consent for genetic research on stored tissue samples

1 reference

12 December 2020

Cystic fibrosis population carrier screening: here at last--are we ready?

1 reference

12 December 2020

Laboratory standards and guidelines for population-based cystic fibrosis carrier screening

1 reference

12 December 2020

PCR-based cystic fibrosis (CF) carrier screening in a first-year medical student biochemistry laboratory.

1 reference

12 December 2020

Rethinking risks to human subjects in genetic research

1 reference

12 December 2020

Commercial molecular diagnostics in the U.S.: The Human Genome Project to the clinical laboratory

1 reference

12 December 2020

Those elusive molecular diagnostics CPT codes

1 reference

12 December 2020

The use and interpretation of commercial APC gene testing for familial adenomatous polyposis

1 reference

12 December 2020

Health insurance and discrimination concerns and BRCA1/2 testing in a clinic population

1 reference

12 December 2020

In the light of preimplantation genetic diagnosis: some ethical issues in medical genetics revisited.

1 reference

12 December 2020

ASHG report. Statement on informed consent for genetic research. The American Society of Human Genetics

1 reference

12 December 2020

Finding a workable balance: regulation of genetic testing in the human genome era.

1 reference

12 December 2020

Use of human tissues in research: clarifying clinician and researcher roles and information flows

1 reference

12 December 2020

Molecular pathology, informed consent, and the paraffin block

1 reference

12 December 2020

Preserving privacy, preventing discrimination becomes the province of genetics experts

1 reference

12 December 2020

Discrimination as a consequence of genetic testing

1 reference

12 December 2020

Cystic fibrosis: molecular diagnosis, population screening, and public policy

1 reference

12 December 2020

The Belmont Report. Ethical principles and guidelines for the protection of human subjects of research

1 reference

12 December 2020

Genetic discrimination and health insurance: an urgent need for reform.

1 reference

12 December 2020

Identifiers

DOI

10.1385/MB:23:2:127

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PubMed ID

12632697

Dimensions Publication ID

6 August 2017

0 references

1 reference

PubMed ID

12632697