Showing results (121-130 of 2,506) with videos related to

Sort By:
Pageof 251
Molecular Genetics & Genomic Medicine|December 22, 2017
Patients with sporadic and familial amyotrophic lateral sclerosis found value in genetic testingKarin N Wagner, Haikady N Nagaraja, Dawn C Allain, et al.
Molecular Genetics & Genomic Medicine|February 6, 2019
Identifying pathogenic variants in the Follistatin-like 1 gene (FSTL1) in patients with skeletal and atrioventricular valve disordersStuti Prakash, Andrea Mattiotti, Marc Sylva, et al.
Molecular Genetics & Genomic Medicine|January 25, 2019
De novo and inherited pathogenic variants in collagen-related osteogenesis imperfectaLidiia Zhytnik, Katre Maasalu, Binh Ho Duy, 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.
Molecular Genetics & Genomic Medicine|January 14, 2019
The promising role of PAX1 (aliases: HUP48, OFC2) gene methylation in cancer screeningChao Fang, Sai-Ying Wang, Yu-Ligh Liou, et al.
Molecular Genetics & Genomic Medicine|February 4, 2019
Canadian genetic healthcare professionals' attitudes towards discussing private pay options with patientsVanessa Di Gioacchino, Sylvie Langlois, Alison M Elliott
Molecular Genetics & Genomic Medicine|January 31, 2019
Tau protein function: The mechanical exploration of axonal transport disorder caused by persistent pressure in dorsal root gangliaLei Zhang, Jun Fu, Xin-Hua Cheng, et al.
Molecular Genetics & Genomic Medicine|January 31, 2019
A multidisciplinary approach to the clinical management of Prader-Willi syndromeJessica Duis, Pieter J van Wattum, Ann Scheimann, et al.
Molecular Genetics & Genomic Medicine|December 28, 2019
Lessons learned from expanded reproductive carrier screening in self-reported Ashkenazi, Sephardi, and Mizrahi Jewish patientsGidon Akler, Ashley H Birch, Nicole Schreiber-Agus, et al.
Molecular Genetics & Genomic Medicine|December 31, 2019
A novel de novo nonsense mutation in ZC4H2 causes Wieacker-Wolff SyndromeDan Wang, Dongjie Hu, Zhichao Guo, et al.
Pageof 251