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