-
[gse89594] Integrated network analysis reveals genotype-phenotype correlation...
Number of resources: 94 (94 raw, 0 normalizations, 0 DE files)Williams Syndrome (WS) is a rare neurodevelopmental disorder caused by heterozygous deletions in a chromosome 7q11.23 region typically encompassing 26-28 genes. WS patients...
Du kan också komma åt katalogen via API (se API-dokumentation).