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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Last updated 10 novembro 2024
A Mosaic Maternal Splice Donor Mutation In The EHMT1 Gene, 59% OFF
A Mosaic Maternal Splice Donor Mutation In The EHMT1 Gene, 59% OFF
EHMT1 Gene - GeneCards, EHMT1 Protein
Short Report in 2012 European Journal of Human Genetics
PDF) A de novo splice site mutation in EHMT1 resulting in
Postzygotic single-nucleotide mosaicisms in whole-genome sequences
A de novo splice site mutation in EHMT1 resulting in Kleefstra
New Insights into Kleefstra Syndrome: Report of Two Novel Cases
An epigenetic framework for neurodevelopmental disorders: From
PDF) Cytogenetic and Molecular Genetic Characterization of
Kleefstra-variant syndrome with heterozygous mutations in EHMT1
Detection of germline mosaicism in fathers of children with
A Novel Kleefstra Syndrome-associated Variant That Affects the
Postzygotic single-nucleotide mosaicisms in whole-genome sequences
A de novo splice site mutation in EHMT1 resulting in Kleefstra
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