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Kidney International|October 22, 2015
Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicityDaniela A Braun, Markus Schueler, Jan Halbritter, et al.American Journal of Human Genetics|January 17, 2017
Mutations in MAPKBP1 Cause Juvenile or Late-Onset Cilia-Independent NephronophthisisMaxence S Macia, Jan Halbritter, Marion Delous, et al.Pediatric Nephrology (Berlin, Germany)|December 1, 2023
Characteristics and predictors of chronic kidney disease in children with myelomeningocele: a nationwide cohort studyÇağla Serpil Doğan, Sevgin Taner, Betül Durucu Tiryaki, et al.Pageof 5