publication venue for
- Therapy development in Huntington disease: From current strategies to emerging opportunities.. 176:842-861. 2017
- Rare inherited A2BP1 deletion in a proband with autism and developmental hemiparesis.. 158A:1654-61. 2012
- Ovarian failure in ataxia with oculomotor apraxia type 2.. 143A:1775-7. 2007
- Access to health insurance: experiences and attitudes of those with genetic versus non-genetic medical conditions.. 143A:707-17. 2007
- Medical privacy and the disclosure of personal medical information: the beliefs and experiences of those with genetic and other clinical conditions.. 128A:261-70. 2004