A New Edition of Genetics in Medicine is Available
January 9, 2014
Genetics in Medicine (Volume 16, No. 1, January 2014) is now available online by subscription only.
Articles include:
- “Public preferences regarding informed consent models for participation in population-based genomic research†by Jodyn Platt, et al.
- “The use of US health insurance data for surveillance of rare disorders: hereditary hemorrhagic telangiectasia†by Scott D. Grosse, et al.
- “Neonatal hypocalcemia, neonatal seizures, and intellectual disability in 22q11.2 deletion syndrome†by Evelyn Ning Man Cheung, et al.
- “A cancer genetics toolkit improves access to genetic services through documentation and use of the family history by primary-care clinicians†by Maren T. Scheuner, et al.
- “Diagnostic yield of array comparative genomic hybridization in adults with autism spectrum disorders†by Gary Stobbe, et al.
- “Parents’ interest in whole-genome sequencing of newborns†by Aaron J. Goldenberg, et al.
- “Variations in predicted risks in personal genome testing for common complex diseases†by Rachel R.J. Kalf, et al.
