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• Brachyolmia type 3
  *Heterozygous mutations in the '''TRPV4 gene (12q24.11)''' are responsible for autosomal dominant brachyolmia.
  4 KB (583 words) - 10:39, 13 January 2021
• Medical-dictionary-0-9
  * [[12q24.11]]
  14 KB (1,362 words) - 02:37, 5 November 2023
• Joubert syndrome
  | 12q24.11
  18 KB (2,379 words) - 03:30, 28 April 2020