A mosaic maternal splice donor mutation in the EHMT1 gene leads to aberrant transcripts and to Kleefstra syndrome in the offspring
Por um escritor misterioso
Descrição
Using whole-exome sequencing to identify variants inherited from
EHMT1 Gene - GeneCards, EHMT1 Protein
An epigenetic framework for neurodevelopmental disorders: From
Hypogonadotropic Hypogonadism and Kleefstra Syndrome due to a
A de novo splice site mutation in EHMT1 resulting in Kleefstra
A Mosaic Maternal Splice Donor Mutation In The EHMT1 Gene, 59% OFF
Short Report in 2012 European Journal of Human Genetics
A Mosaic Maternal Splice Donor Mutation In The EHMT1 Gene, 59% OFF
Postzygotic single-nucleotide mosaicisms in whole-genome sequences
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por adulto (o preço varia de acordo com o tamanho do grupo)