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Cancer Genetics|June 2, 2016
Whole-exome identifies RXRG and TH germline variants in familial isolated prolactinomaFlavia M Melo, Patrícia P Couto, Allen E Bale, et al.Circulation. Cardiovascular Genetics|January 15, 2017
Application of Whole Exome Sequencing in the Clinical Diagnosis and Management of Inherited Cardiovascular Diseases in AdultsSara B Seidelmann, Emily Smith, Lakshman Subrahmanyan, et al.Hepatology (Baltimore, Md.)|August 31, 2010
A common variant in the patatin-like phospholipase 3 gene (PNPLA3) is associated with fatty liver disease in obese children and adolescentsNicola Santoro, Romy Kursawe, Ebe D'Adamo, et al.Cancer Research|September 20, 2006
Cytogenetic instability in ovarian epithelial cells from women at risk of ovarian cancerTanja Pejovic, Jane E Yates, Hong Y Liu, et al.Cell|June 14, 1996
Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndromeH Hahn, C Wicking, P G Zaphiropoulous, et al.Blood Advances|January 4, 2018
Whole-exome sequencing in evaluation of patients with venous thromboembolismEun-Ju Lee, Daniel J Dykas, Andrew D Leavitt, et al.Genetics in Medicine Open|August 23, 2024
The challenges and opportunities of offering and integrating training in clinical molecular genetics and clinical cytogenetics: A survey of LGG Fellowship Program DirectorsJoshua L Deignan, Vimla Aggarwal, Allen E Bale, et al.Proceedings of the National Academy of Sciences of the United States of America|October 19, 2011
Loss-of-function mutations in Notch receptors in cutaneous and lung squamous cell carcinomaNicholas J Wang, Zachary Sanborn, Kelly L Arnett, et al.British Journal of Cancer|January 26, 2008
Progesterone receptor variation and risk of ovarian cancer is limited to the invasive endometrioid subtype: results from the Ovarian Cancer Association Consortium pooled analysisC L Pearce, A H Wu, S A Gayther, et al.Journal of the American Academy of Dermatology|December 15, 2025
Clinical practice guidelines for the management of basal cell carcinoma in Gorlin syndromeBrian A Cahn, Runze Zhang, Allie M Sidwell, et al.Pageof 13