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Browsing Articles by Subject "whole exome sequencing"

Browsing Articles by Subject "whole exome sequencing"

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  • T. van der Ven, Amelie; Kobbe, Birgit; Kohl, Stefan; Shril, Shirlee; Pogoda, Hans-Martin; Imhof, Thomas; Ityel, Hadas; Vivante, Asaf; Chen, Jing; Hwang, Daw-Yang; M. Connaughton, Dervla; Mann, Nina; Widmeier, Eugen; Taglienti, Mary; Schmidt, Johanna Magdalena; Nakayama, Makiko; Senguttuvan, Prabha; Kumar, Selvin; Tasic, Velibor; Kehinde, Elijah O.; M. Mane, Shrikant; P. Lifton, Richard; Soliman, Neveen; Lu, Weining; B. Bauer, Stuart; Hammerschmidt, Matthias; Wagener, Raimund; Hildebrandt, Friedhelm (Public Library of Science, 2018-01)
    Congenital anomalies of the kidney and urinary tract (CAKUT) are the most common cause (40–50%) of chronic kidney disease (CKD) in children. About 40 monogenic causes of CAKUT have so far been discovered. To date less than ...

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