Found: 32
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Caregivers' perception of and experience with variants of uncertain significance from whole exome sequencing for children with undiagnosed conditions.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 304, doi. 10.1002/jgc4.1093
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Role and practice evolution for genetic counseling in the genomic era: The experience of Australian and UK genetics practitioners.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 378, doi. 10.1002/jgc4.1053
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Genetic counseling, 2030: An on‐demand service tailored to the needs of a price conscious, genetically literate, and busy world.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 456, doi. 10.1002/jgc4.1123
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New developmental syndromes: Understanding the family experience.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 202, doi. 10.1002/jgc4.1121
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A toolkit for genetics providers in follow‐up of patients with non‐diagnostic exome sequencing.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 213, doi. 10.1002/jgc4.1119
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Understanding the present and preparing for the future: Exploring the needs of diagnostic and elective genomic medicine patients.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 438, doi. 10.1002/jgc4.1114
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- Article
Rapid clinical exome sequencing in a pediatric ICU: Genetic counselor impacts and challenges.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 283, doi. 10.1002/jgc4.1116
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- Article
Genetics professionals' attitudes toward prenatal exome sequencing.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 229, doi. 10.1002/jgc4.1112
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INTRODUCTION TO EXPLORING THE EXOME SPECIAL ISSUE.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 181, doi. 10.1002/jgc4.1113
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- Article
A novel approach to offering additional genomic findings—A protocol to test a two‐step approach in the healthcare system.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 388, doi. 10.1002/jgc4.1102
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Genetic counseling for consumer‐driven whole exome and whole genome sequencing: A commentary on early experiences.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 449, doi. 10.1002/jgc4.1109
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- Article
Readiness of clinical genetic healthcare professionals to provide genomic medicine: An Australian census.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 367, doi. 10.1002/jgc4.1101
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- Article
Perspectives on facilitating whole exome sequencing for international patients at Mayo Clinic.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 398, doi. 10.1002/jgc4.1100
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Much ado about nothing: A qualitative study of the experiences of an average‐risk population receiving results of exome sequencing.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 428, doi. 10.1002/jgc4.1096
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- Article
Factors complicating the informed consent process for whole exome sequencing in neonatal and pediatic intensive care units.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 256, doi. 10.1002/jgc4.1097
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- Article
Secondary findings: How did we get here, and where are we going?
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 326, doi. 10.1002/jgc4.1098
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- Article
Developing a genomics rotation: Practical training around variant interpretation for genetic counseling students.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 466, doi. 10.1002/jgc4.1094
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- Article
Beyond medical actionability: Public perceptions of important actions in response to hypothetical genetic testing results.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 355, doi. 10.1002/jgc4.1048
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Cases from the Undiagnosed Diseases Network: The continued value of counseling skills in a new genomic era.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 194, doi. 10.1002/jgc4.1091
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Using the diffusion of innovations model to guide participant engagement in the genomics era.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 419, doi. 10.1002/jgc4.1090
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- Article
Genetic counseling in pediatric acute care: Reflections on ultra‐rapid genomic diagnoses in neonates.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 273, doi. 10.1002/jgc4.1086
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Genetic counselors' perceptions of uncertainty in pretest counseling for genomic sequencing: A qualitative study.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 292, doi. 10.1002/jgc4.1076
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Patients' perspectives of variants of uncertain significance and strategies for uncertainty management.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 313, doi. 10.1002/jgc4.1075
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Genetic counseling considerations with rapid genome‐wide sequencing in a neonatal intensive care unit.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 263, doi. 10.1002/jgc4.1074
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Indigenous Peoples and genomics: Starting a conversation.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 407, doi. 10.1002/jgc4.1073
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User Acceptability of Whole Exome Reproductive Carrier Testing for Consanguineous Couples in Australia.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 240, doi. 10.1007/s10897-018-0298-5
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Interpretations of the Term "Actionable" when Discussing Genetic Test Results: What you Mean Is Not What I Heard.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 334, doi. 10.1007/s10897-018-0289-6
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Lay Perspectives on Receiving Different Types of Genomic Secondary Findings: a Qualitative Vignette Study.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 343, doi. 10.1007/s10897-018-0288-7
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The Feelings About genomiC Testing Results (FACToR) Questionnaire: Development and Preliminary Validation.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 477, doi. 10.1007/s10897-018-0286-9
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Comparison of medical management and genetic counseling options pre‐ and post‐whole exome sequencing for patients with positive and negative results.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 182, doi. 10.1002/jgc4.1054
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Issue Information.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 177, doi. 10.1002/jgc4.1001
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- Article
Whole exome sequencing for prenatal diagnosis in cases with fetal anomalies: Criteria to improve diagnostic yield.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 251, doi. 10.1002/jgc4.1045
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- Article