1. Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods. (26th April 2017) Authors: Artieri, Carlo G.; Haverty, Carrie; Evans, Eric A.; Goldberg, James D.; Haque, Imran S.; Yaron, Yuval; Muzzey, Dale Journal: Prenatal diagnosis Issue: Volume 37:Number 5(2017) Page Start: 482 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Noninvasive prenatal screening for patients with high body mass index: Evaluating the impact of a customized whole genome sequencing workflow on sensitivity and residual risk. (20th December 2019) Authors: Muzzey, Dale; Goldberg, James D.; Haverty, Carrie Journal: Prenatal diagnosis Issue: Volume 40:Number 3(2020) Page Start: 333 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Results of the Genetic Counselor SARS‐CoV‐2 Impact Survey from the National Society of Genetic Counselors: Progress and penalty during the COVID‐19 pandemic. Issue 4 (26th July 2021) Authors: Pan, Vivian; Doerr, Megan; Hoell, Christin; Ryan, Lauren; Erwin, Deanna J.; Hooker, Gillian; Haverty, Carrie Journal: Journal of genetic counseling Issue: Volume 30:Issue 4(2021) Page Start: 989 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Response to "Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods". (July 2017) Authors: Muzzey, Dale; Haverty, Carrie; Evans, Eric A.; Goldberg, James D. Journal: Prenatal diagnosis Issue: Volume 37:Number 7(2017) Page Start: 727 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗