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
Last updated 11 novembro 2024
Splice Modulating Therapies for Human Disease: Cell
A mosaic maternal splice donor mutation in the EHMT1 gene leads to
A Mosaic Maternal Splice Donor Mutation In The EHMT1 Gene, 59% OFF
A Mosaic Maternal Splice Donor Mutation In The EHMT1 Gene, 59% OFF
A de novo splice site mutation in EHMT1 resulting in Kleefstra
PDF) A de novo splice site mutation in EHMT1 resulting in
G9a and G9a-Like Histone Methyltransferases and Their Effect on
Kleefstra Syndrome - GeneReviews® - NCBI Bookshelf
Short Report European Journal of Human Genetics
A Mosaic Maternal Splice Donor Mutation In The EHMT1 Gene, 59% OFF
Kleefstra syndrome: Recurrence in siblings due to a paternal
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