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De novo heterozygous variants in SLC30A7 are a candidate cause for Joubert syndrome
Download from onlinelibrary.wiley.comA human cell atlas of fetal gene expression
UploadA human cell atlas of fetal chromatin accessibility
UploadDysfunction of the ciliary ARMC9/TOGARAM1 protein module causes Joubert syndrome
Download from doi.orgCerebellar Watershed Injury in Children
UploadHealthcare recommendations for Joubert syndrome
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