CHD7 functions in the nucleolus as a positive regulator of ribosomal RNA biogenesis. (1/20)

Delayed puberty due to a novel mutation in CHD7 causing CHARGE syndrome. (2/20)

Mutations in the CHD7 gene: the experience of a commercial laboratory. (3/20)

Reproductive dysfunction and decreased GnRH neurogenesis in a mouse model of CHARGE syndrome. (4/20)

The DNA-binding domain of the Chd1 chromatin-remodelling enzyme contains SANT and SLIDE domains. (5/20)

The role of CHD7 and the newly identified WDR11 gene in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndrome. (6/20)

Mature middle and inner ears express Chd7 and exhibit distinctive pathologies in a mouse model of CHARGE syndrome. (7/20)

Chd7 plays a critical role in controlling left-right symmetry during zebrafish somitogenesis. (8/20)

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