Charu Kaiwar

4PUBLICATIONS
18CO-AUTHORS
GenomicsGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Vision science
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Publications (4)

|Feb 10, 2019
Clinical spectrum of STX1B-related epileptic disorders.

Stefan Wolking, Patrick May, Davide Mei

|Jan 26, 2019
De novo variants in FBXO11 cause a syndromic form of intellectual disability with behavioral problems and dysmorphisms.

Sandra Jansen, Ilse M van der Werf, A Micheil Innes

|Dec 15, 2018
A case of YY1-associated syndromic learning disability or Gabriele-de Vries syndrome with myasthenia gravis.

Joel A Morales-Rosado, Charu Kaiwar, Benn E Smith

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