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Journal of Genetic Counseling|August 29, 2015
Newborn Screening for Lysosomal Storage Disorders: Views of Genetic Healthcare ProvidersEmily C Lisi, Shawn E McCandless
Molecular Genetics and Metabolism|September 5, 2016
Patients' perspectives on newborn screening for later-onset lysosomal storage diseasesEmily C Lisi, Scott Gillespie, Dawn Laney, et al.
Journal of Community Genetics|July 22, 2026
Healthcare experiences and the cycle of genomic healthcare disparities: A cross-sectional study utilizing the 'All of Us' research programMegan D Johnson, Aubrey Hite, Jennifer Richmond, et al.
European Journal of Medical Genetics|May 23, 2009
3q29 interstitial microdeletion syndrome: an inherited case associated with cardiac defect and normal cognitionFeng Li, Emily C Lisi, Elizabeth S Wohler, et al.
Pediatric Neurology|October 2, 2007
Albinism and developmental delay: the need to test for 15q11-q13 deletionReem Saadeh, Emily C Lisi, Denise A S Batista, et al.
American Journal of Medical Genetics. Part A|February 5, 2008
3q29 interstitial microduplication: a new syndrome in a three-generation familyEmily C Lisi, Ada Hamosh, Kimberly F Doheny, et al.
Mayo Clinic Proceedings|April 23, 2021
Clinically Actionable Findings Derived From Predictive Genomic Testing Offered in a Medical Practice SettingJennifer L Anderson, Teresa M Kruisselbrink, Emily C Lisi, et al.
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