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2. Exome survey of individuals affected by VATER/VACTERL with renal phenotypes identifies phenocopies and novel candidate genes. Issue 12 (2nd August 2021)

3. Genetic variants in the LAMA5 gene in pediatric nephrotic syndrome. Issue 3 (9th March 2018)

4. Mutations in WDR4 as a new cause of Galloway–Mowat syndrome. Issue 11 (6th August 2018)

5. Panel sequencing distinguishes monogenic forms of nephritis from nephrosis in children. Issue 3 (21st March 2018)