Found: 8
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The Changing Age of Individuals Seeking Presymptomatic Genetic Testing for Huntington Disease.
- Published in:
- Journal of Genetic Counseling, 2018, v. 27, n. 5, p. 1157, doi. 10.1007/s10897-018-0233-9
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- Publication type:
- Article
Implementing a breast cancer registry and treatment plan/summary program in clinical practice: A pilot program.
- Published in:
- Cancer (0008543X), 2013, v. 119, n. 1, p. 158, doi. 10.1002/cncr.27625
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- Publication type:
- Article
Patient perspectives on breast cancer treatment plan and summary documents in community oncology care: a pilot program.
- Published in:
- 2013
- By:
- Publication type:
- journal article
Patient perspectives on breast cancer treatment plan and summary documents in community oncology care.
- Published in:
- Cancer (0008543X), 2013, v. 119, n. 1, p. 164, doi. 10.1002/cncr.27856
- By:
- Publication type:
- Article
Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment.
- Published in:
- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 6, p. 1298, doi. 10.1002/ajmg.a.33970
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- Publication type:
- Article
Vestibular dysfunction in DFNB1 deafness.
- Published in:
- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 5, p. 993, doi. 10.1002/ajmg.a.33828
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- Publication type:
- Article
Fitness Among Individuals with Early Childhood Deafness: Studies in Alumni Families from Gallaudet University.
- Published in:
- Annals of Human Genetics, 2010, v. 74, n. 1, p. 27, doi. 10.1111/j.1469-1809.2009.00553.x
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- Publication type:
- Article
Provision of Genetic Services for Hearing Loss: Results from a National Survey and Comparison to Insights Obtained from Previous Focus Group Discussions.
- Published in:
- Journal of Genetic Counseling, 2009, v. 18, n. 6, p. 618, doi. 10.1007/s10897-009-9246-8
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- Publication type:
- Article