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- {{PAGENAME}} - human pax6 wild type allele is located in the vicinity of 11p13 and is approximately 29 kb in length. This allele, which encodes paired box360 bytes (54 words) - 12:34, 5 April 2024
- ...syndrome involves deletions of several adjacent genes in chromosome region 11p13. ...syndrome is deletion of a group of genes located on chromosome number 11 (11p13 - the "p13" refers to the specific place on chromosome 11 that is affected)9 KB (1,360 words) - 19:04, 23 August 2021
- | 11p13-p123 KB (317 words) - 12:54, 22 February 2024
- ...primarily caused by mutations in the [[PAX6]] gene, located on chromosome 11p13. The PAX6 gene plays a crucial role in the development of the eyes and othe3 KB (424 words) - 12:55, 22 March 2024
- ...involves mutations in several genes, including WT1, located on chromosome 11p13. The WT1 gene plays a crucial role in kidney and gonadal development. Mutat3 KB (473 words) - 20:54, 30 March 2024
- The ''WT1'' gene is located on chromosome 11p13 and consists of 10 [[exon]]s. Mutations in this gene can lead to several ty3 KB (506 words) - 17:19, 24 April 2024
- ...enetic disorder. Studies suggest that certain regions on '''chromosome 11 (11p13) and chromosome 15 (15q14)''' may be involved in BRE, but a specific gene h3 KB (509 words) - 11:08, 10 March 2021
- ...ns in the Wilms tumor suppressor gene, WT1, which is on [[chromosome 11]] (11p13). These mutations are usually found in exons 8 or 9, but at least one has b4 KB (480 words) - 15:20, 18 September 2019
- * [[11p13 p12]]14 KB (1,362 words) - 02:37, 5 November 2023