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Molecular Genetics & Genomic Medicine|July 26, 2018
Personalized molecular modeling for pinpointing associations of protein dysfunction and variants associated with hereditary cancer syndromesSarah Macklin, Ahmed Mohammed, Jessica Jackson, et al.
Human Genome Variation|July 14, 2018
Novel variants in COL4A4 and COL4A5 are rare causes of FSGS in two unrelated familiesStephanie L Hines, Anjali Agarwal, Mohamedanwar Ghandour, et al.
Human Genome Variation|September 6, 2018
Correction: Novel variants in COL4A4 and COL4A5 are rare causes of FSGS in two unrelated familiesStephanie L Hines, Anjali Agarwal, Mohamedanwar Ghandour, et al.
Southern Medical Journal|September 3, 2015
Educational Intervention in Primary Care Residents' Knowledge and Performance of Hepatitis B Vaccination in Patients with Diabetes MellitusSaowanee Ngamruengphong, Jennifer L Horsley-Silva, Stephanie L Hines, et al.
Molecular Genetics & Genomic Medicine|January 30, 2019
Protein informatics combined with multiple data sources enriches the clinical characterization of novel TRPV4 variant causing an intermediate skeletal dysplasiaStephanie L Hines, John E Richter, Ahmed N Mohammad, et al.
SN Comprehensive Clinical Medicine|January 20, 2021
Symptoms and Clinical Outcomes of Coronavirus Disease 2019 in the Outpatient SettingDacre Knight, Katheryne Downes, Bala Munipalli, et al.
International Journal of Surgical Oncology|August 2, 2012
Ductal carcinoma in situ of the breastRichard J Lee, Laura A Vallow, Sarah A McLaughlin, et al.
Journal of Genetic Counseling|December 8, 2022
Patient uptake of updated genetic testing following uninformative BRCA1 and BRCA2 resultsSarah K Macklin-Mantia, Kristin E Clift, Santo Maimone, et al.
Geriatrics|June 3, 2008
A practical approach to guide clinicians in the evaluation of male patients with breast massesStephanie L Hines, Winston Tan, Jan M Larson, et al.
European Journal of Radiology|March 22, 2023
MRI phenotypes associated with breast cancer predisposing genetic variants, a multisite reviewSanto Maimone, Laura K Harper, Sarah K Mantia, et al.
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