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 24 abril 2025


A mosaic maternal splice donor mutation in the EHMT1 gene leads to

Andreas Tzschach's research works
Hypogonadotropic Hypogonadism and Kleefstra Syndrome due to a
A de novo splice site mutation in EHMT1 resulting in Kleefstra

A Novel Kleefstra Syndrome-associated Variant That Affects the

Hypogonadotropic Hypogonadism and Kleefstra Syndrome due to a
EHMT1 Gene - GeneCards, EHMT1 Protein

Kleefstra syndrome: Recurrence in siblings due to a paternal

A mosaic maternal splice donor mutation in the EHMT1 gene leads to

A Novel Kleefstra Syndrome-associated Variant That Affects the
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