A New Edition of Genetics in Medicine Is Now Available

January 17, 2017

Genetics in Medicine (vol. 18, no. 12, 2016) is available online by subscription only.

Articles include:

  • “Newborn Genetic Screening for Hearing Impairment: A Population-Based Longitudinal Study” by Chen-Chi Wu et al
  • “Variants of Uncertain Significance in Newborn Screening Disorders: Implications for Large-Scale Genomic Sequencing” by Alekhya Narravula, Kathryn B. Garber, S. Hussain Askree, Madhuri Hegde, and Patricia L. Hall
  • “Comprehensive Genetic Analysis of Pregnancy Loss by Chromosomal Microarrays: Outcomes, Benefits, and Challenges” by Trilochan Sahoo et al
  • “Newborn Screening for X-Linked Adrenoleukodystrophy: Evidence Summary and Advisory Committee Recommendation” by Alex R. Kemper et al

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