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
Intellectual disability due to monoallelic variant in GATAD2B and
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A mosaic maternal splice donor mutation in the EHMT1 gene leads to
Reprogramming of the epigenome in neurodevelopmental disorders
Detection of germline mosaicism in fathers of children with
Andreas Tzschach's research works
A Novel Kleefstra Syndrome-associated Variant That Affects the
Splice Modulating Therapies for Human Disease: Cell
A Mosaic Maternal Splice Donor Mutation In The EHMT1 Gene, 59% OFF
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