Volume 22, Issue 1, February 2013

ISSN: 1059-7700 (Print) 1573-3599 (Online)

In this issue (16 articles)

  1. No Access

    Events

    Introduction

    Rebecca Nagy Pages 1-3
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  2. No Access

    Professional Development Paper

    NSGC Practice Guideline: Prenatal Screening and Diagnostic Testing Options for Chromosome Aneuploidy

    K. L. Wilson, J. L. Czerwinski, J. M. Hoskovec… Pages 4-15
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  3. No Access

    Professional Issues

    Enhancing Family Communication About Genetics: Ethical and Professional Dilemmas

    Jan Hodgson, Clara Gaff Pages 16-21
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  4. No Access

    Case Presentation

    Unintended Diagnosis of Von Hippel Lindau Syndrome Using Array Comparative Genomic Hybridization (CGH): Counseling Challenges Arising from Unexpected Information

    Jennifer Hogan, A. Turner, K. Tucker, L. Warwick Pages 22-26
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  5. No Access

    Case Presentation

    A Multi-Case Report of the Pathways To and Through Genetic Testing and Cancer Risk Management for BRCA Mutation-Positive Women Aged 18–25

    Lindsey M. Hoskins, Allison Werner-Lin Pages 27-38
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  6. No Access

    Original Research

    Genetic Counseling Supervisor Competencies: Results of a Delphi Study

    Sonja Eubanks Higgins, Patricia McCarthy Veach… Pages 39-57
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  7. No Access

    Original Research

    Effects of Second Language Usage on Genetic Counseling Training and Supervision

    Rachel Vanneste, Sui Mei Chiu, Laura Russell… Pages 58-75
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  8. No Access

    Original Research

    Prenatal Genetic Testing: An Investigation of Determining Factors Affecting the Decision-Making Process

    Monica Pivetti, Giannino Melotti Pages 76-89
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  9. No Access

    Original Research

    Attitudes and Practices Among Internists Concerning Genetic Testing

    Robert Klitzman, Wendy Chung, Karen Marder… Pages 90-100
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  10. No Access

    Original Research

    Factors Associated with Psychological Distress among Women of African Descent at High Risk for BRCA Mutations

    Yael R. Cukier, Hayley S. Thompson, Katarina Sussner… Pages 101-107
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  11. No Access

    Original Research

    Design and Evaluation of a Decision Aid for Inviting Parents to Participate in a Fragile X Newborn Screening Pilot Study

    Donald B. Bailey Jr., Megan A. Lewis, Shelly L. Harris… Pages 108-117
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  12. Original Research

    Focusing on Patient Needs and Preferences May Improve Genetic Counseling for Colorectal Cancer

    Simone Salemink, Nicky Dekker, Carolien M. Kets… Pages 118-124
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  13. No Access

    Original Research

    A Mobile Colonoscopic Unit for Lynch Syndrome: Trends in Surveillance Uptake and Patient Experiences of Screening in a Developing Country

    Zandrè Bruwer, Merle Futter, Raj Ramesar Pages 125-137
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  14. No Access

    Original Research

    “Is it Really Worth it to Get Tested?”: Primary Care Patients’ Impressions of Predictive SNP Testing for Colon Cancer

    Kara-Grace Leventhal, William Tuong, Beth N. Peshkin… Pages 138-151
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  15. No Access

    Letter to the Editor

    Response to Article: Langford et al. Racial and Ethnic Differences in Direct-to-Consumer Genetic Tests Awareness in HINTS 2007: Sociodemographic and Numeracy Correlates. J Genet Counsel (2012) 21:440–447

    Shelly Cummings Pages 152-153
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  16. Letter to the Editor

    Response to Letter Written by Shelly Cummings, MS, CGC of Myriad Genetics Laboratories, Inc. Regarding the Paper, “Racial and Ethnic Differences in Direct-to-Consumer Genetic Tests Awareness in HINTS 2007: Sociodemographic and Numeracy Correlates.” J Genet Counsel (2012) 21:440-447

    Aisha T. Langford, Ken Resnicow, J. Scott Roberts… Page 154
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