A mosaic maternal splice donor mutation in the EHMT1 gene leads to aberrant transcripts and to Kleefstra syndrome in the offspring
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A Mosaic Maternal Splice Donor Mutation In The EHMT1 Gene, 59% OFF

Detection of germline mosaicism in fathers of children with

New Insights into Kleefstra Syndrome: Report of Two Novel Cases

Reprogramming of the epigenome in neurodevelopmental disorders

A Mosaic Maternal Splice Donor Mutation In The EHMT1 Gene, 59% OFF

A mosaic maternal splice donor mutation in the EHMT1 gene leads to
A de novo splice site mutation in EHMT1 resulting in Kleefstra

EHMT1 Gene - GeneCards, EHMT1 Protein

Genes, Free Full-Text

Reprogramming of the epigenome in neurodevelopmental disorders

A Mosaic Maternal Splice Donor Mutation In The EHMT1 Gene, 59% OFF

Reversible white matter lesions associated with mutant EHMT1 and

PDF) A de novo splice site mutation in EHMT1 resulting in

Aberrant splicing events caused by insertion of genes of interest
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