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Accession Title Series type(s) Organism(s) Samples GDS Supplementary Contact Release date
Remove filtersFilter Remove filterTXT Remove filterMuhammad Sajid Hussain
GSE190621
Biallelic variant in LEF1 are associated with a new syndrome combining ectodermal dysplasia and limb malformations through altered WNT signalling
4 Muhammad Sajid Hussain Dec 01, 2023
GSE189065
De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway
4 Muhammad Sajid Hussain Apr 28, 2022