Showing results (1571-1580 of 1,657) with videos related to

Sort By:
Pageof 166
Journal of the American Society of Nephrology : JASN|February 17, 2021
Mutations in <i>PRDM15</i> Are a Novel Cause of Galloway-Mowat SyndromeNina Mann, Slim Mzoughi, Ronen Schneider, et al.
Neuron|December 19, 2014
Mutations in KATNB1 cause complex cerebral malformations by disrupting asymmetrically dividing neural progenitorsKetu Mishra-Gorur, Ahmet Okay Çağlayan, Ashleigh E Schaffer, et al.
American Journal of Human Genetics|May 31, 2016
Loss-of-Function Mutations in FRRS1L Lead to an Epileptic-Dyskinetic EncephalopathyMarianna Madeo, Michelle Stewart, Yuyang Sun, et al.
Nucleic Acids Research|December 5, 2006
PATRIC: the VBI PathoSystems Resource Integration CenterE E Snyder, N Kampanya, J Lu, et al.
Science (New York, N.Y.)|January 20, 2016
De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomaliesJason Homsy, Samir Zaidi, Yufeng Shen, et al.
Kidney International|September 13, 2017
Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosisAnkana Daga, Amar J Majmundar, Daniela A Braun, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 30, 2016
Mutational landscape of uterine and ovarian carcinosarcomas implicates histone genes in epithelial-mesenchymal transitionSiming Zhao, Stefania Bellone, Salvatore Lopez, et al.
Kidney International|February 19, 2019
Monogenic causes of chronic kidney disease in adultsDervla M Connaughton, Claire Kennedy, Shirlee Shril, et al.
Pageof 166