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Dataset of differentially expressed genes from SOX9 over-expressing NT2/D1 cells.

artículo científico publicado en 2016

Functional characterisation of a novel PBX1 de novo missense variant identified in a patient with syndromic congenital heart disease

scientific article published on 18 October 2019

Identification of clinically actionable variants from genome sequencing of families with congenital heart disease

scientific article published on 08 October 2018

Myhre syndrome is caused by dominant-negative dysregulation of SMAD4 and other co-factors

artículo científico publicado en 2022

SOX9 regulates expression of the male fertility gene Ets variant factor 5 (ETV5) during mammalian sex development.

artículo científico publicado en 2016

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