| Accession | Title | Series type(s) | Organism(s) | Samples | GDS | Supplementary | Contact | Release date |
|---|---|---|---|---|---|---|---|---|
 Filter
|
Expression profiling by high throughput sequencing
|
TXT
|
Muhammad 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 |
