Don Bailey

RTI uses cookies to offer you the best experience online. By clicking “accept” on this website, you opt in and you agree to the use of cookies. If you would like to know more about how RTI uses cookies and how to manage them please view our Privacy Policy here. You can “opt out” or change your mind by visiting: http://optout.aboutads.info/. Click “accept” to agree.

Search Results

Filter

Filter by Type

Filter by Focus Area

Filter by Center

Search Results

New laboratory screening test for fragile X syndrome shortly after birth now ready for pivotal North Carolina Early Check clinical study

A digital health app to assess decisional capacity to provide informed consent: Protocol for a randomized controlled trial

Developmental trajectories of executive functions in young males with fragile X syndrome

New NC-Based Study to Advance Research Through Free and Expanded Health Screening for Newborn Babies

Skills attained by infants with congenital Zika syndrome: Pilot data from Brazil

Family impact of congenital Zika syndrome likely to last a lifetime

Parental preferences toward genomic sequencing for non-medically actionable conditions in children: A discrete-choice experiment

A comparison of functional academic and daily living skills in males with fragile X syndrome with and without autism

RTI International to serve as partner on nationwide screening and education program for Severe Combined Immunodeficiency

A digital decision support tool to enhance decisional capacity for clinical trial consent: Design and development

RTI International, UNC and partners receive NIH Clinical & Translational Science Award renewal

Evaluating parents' decisions about next-generation sequencing for their child in the NC NEXUS (North Carolina Newborn Exome Sequencing for Universal Screening) study: A randomized controlled trial protocol

Values clarification exercises improved parental decision making about newborn genomic sequencing

You can get your baby tested for two rare genetic disorders - for free

Early check: A voluntary newborn screening program and research registry to facilitate clinical trials in pre-symptomatic infants with rare diseases

The likely impact of congenital zika syndrome on families: Considerations for family supports and services

Decision making in couples offered genomic sequencing for newborn screening: Outcomes of a surrogate, joint decision