Jens Michael Hertz
4PUBLICATIONS
3CO-AUTHORS
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Publications (4)
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|Feb 25, 2022
Detection of DZIP1L mutations by whole-exome sequencing in consanguineous families with polycystic kidney disease.Jens Michael Hertz, Per Svenningsen, Henrik Dimke
|Sep 21, 2020
Biallelic variants in GLE1 with survival beyond neonatal period.T Michael Yates, Philippe M Campeau, Jamal Ghoumid
|Aug 20, 2020
Low frequency of parental mosaicism in de novo COL4A5 mutations in X-linked Alport syndrome.Ole Magnus Bjorgaas Helle, Torkild Høieggen Pedersen, Lilian Bomme Ousager
|Apr 14, 2019
A novel PDGFRB sequence variant in a family with a mild form of primary familial brain calcification: a case report and a review of the literature.Stine Westergaard Mathorne, Kristina Sørensen, Christina Fagerberg
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