1. Genetic Testing: Understanding the Personal Stories
  2. James M. DuBois
  3. pp. 201-203
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  1. Ethical Issues in Interpretation of Risk, from the Perspective of a Research Subject
  2. Dena Davis
  3. pp. 203-206
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  1. Whole Genome Sequencing Solved Our Family’s Genetic Mystery: Titin
  2. Sarah Foye
  3. pp. 206-208
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  1. My Experience with Direct to Consumer Genetic Testing
  2. Sarah M. Hartz
  3. pp. 208-210
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  1. Illusions of Certainty
  2. Carla C. Keirns
  3. pp. 210-212
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  1. 23andMe and Me
  2. Christopher M. Lietz
  3. pp. 212-214
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  1. I Had Genetic Testing for Alzheimer’s Disease Without My Consent
  2. Anneke Lucassen
  3. pp. 214-216
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  1. A Test Unlike Any Other
  2. Jacqueline Savard
  3. pp. 216-218
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  1. Becoming the “Subject” of My Own Study
  2. KA Strong
  3. pp. 219-220
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  1. “Welcome to You”: A Reflection on Genetic Self-Exploration
  2. Kiri Sunde
  3. pp. 220-222
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  1. Peering into Vulnerable Genes: Genetic Risk and Population Screening
  2. Michael J. Young
  3. pp. 222-224
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  1. The Impact of My Genetic Testing on My Father
  2. Anonymous One
  3. pp. 224-226
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  1. A Sister, a Father and a Son: Autism, Genetic Testing, and Impossible Decisions
  2. Anonymous Two
  3. pp. 226-228
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  1. Personal Narratives of Genetic Testing: Expectations, Emotions, and Impact on Self and Family
  2. Emily E. Anderson, Katherine Wasson
  3. pp. 229-235
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  1. In Guanine We Trust: Genetic Testing and the Sense of Coherence
  2. James M. DuBois, Alison L. Antes
  3. pp. 237-244
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  1. Appreciating Uncertainty and Personal Preference in Genetic Testing
  2. Adam Kadlac
  3. pp. 245-249
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  1. Physician Religion and End–of–Life Pediatric Care: A Qualitative Examination of Physicians’ Perspectives
  2. Lori Brand Bateman, Jeffrey Michael Clair
  3. pp. 251-269
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  1. System Failure: No Surgeon To Be Found
  2. Carol Bayley
  3. pp. 271-277
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  1. Editors’ Note
  2. James M. DuBois, Ana S. Ilitis, Susan G. DuBois
  3. p. v
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