Found: 16
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Using the diffusion of innovations model to guide participant engagement in the genomics era.
- Published in:
- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 419, doi. 10.1002/jgc4.1090
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- Article
TUBB3 Arg262His causes a recognizable syndrome including CFEOM3, facial palsy, joint contractures, and early-onset peripheral neuropathy.
- Published in:
- Human Genetics, 2021, v. 140, n. 12, p. 1709, doi. 10.1007/s00439-021-02379-9
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- Article
Applications of artificial intelligence in clinical laboratory genomics.
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- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2023, v. 193, n. 3, p. 1, doi. 10.1002/ajmg.c.32057
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- Article
Cover Image, Volume 193, Number 3, September 2023.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2023, v. 193, n. 3, p. 1, doi. 10.1002/ajmg.c.31982
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- Article
Genetic testing outcomes in a cohort of 21,159 children with heart disease.
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- Cardiology in the Young, 2022, v. 32, n. S2, p. S3, doi. 10.1017/S1047951122001950
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- Article
The genetics of familial lymphomas.
- Published in:
- Current Oncology Reports, 2004, v. 6, n. 5, p. 380, doi. 10.1007/s11912-004-0064-8
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- Article
Differentiating Moebius syndrome and other congenital facial weakness disorders with electrodiagnostic studies.
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- Muscle & Nerve, 2021, v. 63, n. 4, p. 516, doi. 10.1002/mus.27159
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- Article
Research participants' attitudes towards the confidentiality of genomic sequence information.
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- European Journal of Human Genetics, 2014, v. 22, n. 8, p. 964, doi. 10.1038/ejhg.2013.276
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- Article
Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 3, p. 261, doi. 10.1038/ejhg.2012.179
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- Article
Motivators for participation in a whole-genome sequencing study: implications for translational genomics research.
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- European Journal of Human Genetics, 2011, v. 19, n. 12, p. 1213, doi. 10.1038/ejhg.2011.123
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- Article
Rates and Classification of Variants of Uncertain Significance in Hereditary Disease Genetic Testing.
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- JAMA Network Open, 2023, v. 6, n. 10, p. e2339571, doi. 10.1001/jamanetworkopen.2023.39571
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- Article
Approaches to informed consent for hypothesis-testing and hypothesis-generating clinical genomics research.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 45, doi. 10.1186/1755-8794-5-45
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- Article
A Genetic Counselor's Guide to Using Next-Generation Sequencing in Clinical Practice.
- Published in:
- Journal of Genetic Counseling, 2014, v. 23, n. 4, p. 455, doi. 10.1007/s10897-013-9662-7
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- Article
Stem Cell Research and Therapy: The Position of the National Society of Genetic Counselors.
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- Journal of Genetic Counseling, 2013, v. 22, n. 4, p. 407, doi. 10.1007/s10897-013-9572-8
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- Article
Noninvasive Prenatal Testing/Noninvasive Prenatal Diagnosis: the Position of the National Society of Genetic Counselors.
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- Journal of Genetic Counseling, 2013, v. 22, n. 3, p. 291, doi. 10.1007/s10897-012-9564-0
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- Article
The TP53 mutational spectrum and frequency of CHEK2*1100delC in Li–Fraumeni-like kindreds.
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- Familial Cancer, 2005, v. 4, n. 2, p. 177, doi. 10.1007/s10689-004-1946-5
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- Article