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1. A heritable microduplication encompassing TBL1XR1 causes a genomic sister‐disorder for the 3q26.32 microdeletion syndrome. Issue 8 (2nd June 2017)

2. A step towards precision medicine in management of severe transient polyhydramnios: MAGED2 variant. (3rd April 2019)

3. Genomic profiling reveals distinctive molecular relapse patterns in IDH1/2 wild‐type glioblastoma. Issue 7 (4th April 2014)

4. Molecular characterization of long‐term survivors of glioblastoma using genome‐ and transcriptome‐wide profiling. Issue 8 (28th March 2014)

5. Mutation Update for Kabuki Syndrome Genes KMT2D and KDM6A and Further Delineation of X‐Linked Kabuki Syndrome Subtype 2. Issue 9 (7th July 2016)