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 02 junho 2024
A Mosaic Maternal Splice Donor Mutation In The EHMT1 Gene, 59% OFF
An epigenetic framework for neurodevelopmental disorders: From
A mosaic maternal splice donor mutation in the EHMT1 gene leads to
Detection of germline mosaicism in fathers of children with
Postzygotic single-nucleotide mosaicisms in whole-genome sequences
EHMT1 Gene - GeneCards, EHMT1 Protein
Postzygotic single-nucleotide mosaicisms in whole-genome sequences
An epigenetic framework for neurodevelopmental disorders: From
Detection of germline mosaicism in fathers of children with
Postzygotic single-nucleotide mosaicisms in whole-genome sequences
PDF) A de novo splice site mutation in EHMT1 resulting in
Reprogramming of the epigenome in neurodevelopmental disorders
Hypogonadotropic Hypogonadism and Kleefstra Syndrome due to a
EHMT1 Gene - GeneCards, EHMT1 Protein
A Mosaic Maternal Splice Donor Mutation In The EHMT1 Gene, 59% OFF
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