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• Odontoma dysphagia syndrome
  ...sphagia syndrome is most likely caused by a microduplication of chromosome 11q13.3, including the FGF3 and FGF4 genes. Clin Oral Investig</ref>
  2 KB (269 words) - 15:05, 1 May 2020
• Distal spinal muscular atrophy type 1
  ...aused by mutations in the [[IGHMBP2]] gene, which is located on chromosome 11q13.3. This condition is inherited in an [[autosomal recessive]] manner, meaning
  3 KB (384 words) - 21:52, 23 April 2024
• Gala
  ...uggesting its evolutionary importance. The GAL gene, located on chromosome 11q13.3-11q13.5 in humans, encodes the galanin peptide. Post-translational processi
  3 KB (383 words) - 10:36, 22 March 2024
• Galanin
  ...essing. The gene responsible for encoding galanin is located on chromosome 11q13.3 in humans. The structure of galanin is characterized by a conserved N-termi
  3 KB (459 words) - 08:34, 22 March 2024
• Otodental syndrome
  ...], a [[microdeletion]] in the Fas-associated death domain ([[FADD]]) gene (11q13.3) was also found to be responsible. There is variable penetrance and variabl ...e are any abnormalities in the [[FGF3]] gene (11q13) or the [[FADD]] gene (11q13.3).<ref name="D"/> Additional tests that can help diagnose otodental syndrome
  12 KB (1,778 words) - 16:37, 9 September 2020
• Medical-dictionary-0-9
  * [[11q13.3 q13.5]]
  14 KB (1,362 words) - 02:37, 5 November 2023