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National Society of Genetic Counselors Code of Ethics: Explication of 2017 Revisions.
- Published in:
- Journal of Genetic Counseling, 2018, v. 27, n. 1, p. 9, doi. 10.1007/s10897-017-0165-9
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- Article
Presented Abstracts from the Thirty Second Annual Education Conference of the National Society of Genetic Counselors (Anaheim, CA, October 2013)
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- 2013
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- Publication type:
- Abstract
SLC26A4 genotype, but not cochlear radiologic structure, is correlated with hearing loss in ears with an enlarged vestibular aqueduct.
- Published in:
- Laryngoscope, 2010, v. 120, n. 2, p. 384, doi. 10.1002/lary.20722
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- Article
Use of SLC26A4 Mutation Testing for Unilateral Enlargement of the Vestibular Aqueduct.
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- JAMA Otolaryngology-Head & Neck Surgery, 2013, v. 139, n. 9, p. 907, doi. 10.1001/jamaoto.2013.4185
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- Article
The relationship between the genetic counseling profession and the disability community: A commentary.
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- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 8, p. 1777, doi. 10.1002/ajmg.a.34054
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- Article
Hypo-Functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: Genotype-phenotype correlation or coincidental polymorphisms?
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- Human Mutation, 2009, v. 30, n. 4, p. 599, doi. 10.1002/humu.20884
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- Article
Factors associated with perceived uncertainty among parents of children with undiagnosed medical conditions.
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- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 8, p. 1877, doi. 10.1002/ajmg.a.35425
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- Article
Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28.
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 23, p. 2877, doi. 10.1093/hmg/11.23.2877
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- Publication type:
- Article