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  • 113 bytes (14 words) - 02:50, 5 April 2024
  • 149 bytes (13 words) - 19:05, 8 April 2024
  • 1 KB (152 words) - 03:54, 30 November 2021
  • '''Acta Oto-Laryngologica''' is a peer-reviewed [[medical journal]] that focuses on the '''Acta Oto-Laryngologica''' publishes original research articles, review articles, and
    2 KB (261 words) - 22:31, 10 March 2024
  • 634 bytes (88 words) - 08:01, 21 March 2024
  • ...:_Autosomal_dominant_-_en.svg| Autosomal dominant - en|thumb]] '''Branchio-oto-renal (BOR) syndrome''' is a genetic disorder that affects the development o
    3 KB (422 words) - 02:28, 24 April 2024
  • '''Oto-Palatal-Digital Syndrome''' (OPD syndrome) is a rare genetic disorder that a The symptoms of Oto-Palatal-Digital Syndrome can vary widely among affected individuals but gene
    3 KB (425 words) - 20:54, 30 March 2024
  • #REDIRECT [[Branchio-oto-renal syndrome]] {{R from other capitalisation}}
    73 bytes (7 words) - 11:42, 20 August 2021
  • ...divided into two main types: Oto-Palato-Digital Syndrome Type 1 (OPD1) and Oto-Palato-Digital Syndrome Type 2 (OPD2), each caused by mutations in the ''FLN ===Oto-Palato-Digital Syndrome Type 1===
    3 KB (498 words) - 02:19, 22 March 2024
  • '''Acro-oto-radial syndrome''' is a rare [[genetic disorder]] characterized by anomalies The primary symptoms of Acro-oto-radial syndrome include [[microtia]] (underdevelopment of the external ear),
    2 KB (301 words) - 15:59, 2 March 2024
  • 6 KB (900 words) - 11:41, 9 October 2020
  • 6 KB (804 words) - 13:21, 9 October 2020

Page text matches

  • #REDIRECT [[Branchio-oto-renal syndrome]]
    41 bytes (3 words) - 11:49, 20 August 2021
  • #REDIRECT [[Branchio-oto-renal syndrome]] {{R from other capitalisation}}
    73 bytes (7 words) - 11:42, 20 August 2021
  • 634 bytes (88 words) - 08:01, 21 March 2024
  • 113 bytes (14 words) - 02:50, 5 April 2024
  • '''Acro-oto-radial syndrome''' is a rare [[genetic disorder]] characterized by anomalies The primary symptoms of Acro-oto-radial syndrome include [[microtia]] (underdevelopment of the external ear),
    2 KB (301 words) - 15:59, 2 March 2024
  • 823 bytes (139 words) - 06:40, 8 April 2024
  • Unlike [[branchio-oto-renal syndrome|branchio-oto-renal (BOR) syndrome]], Lachiewicz–Sibley syndrome is characterized by onl * [[Branchio-oto-renal syndrome]]
    2 KB (206 words) - 15:43, 9 September 2020
  • '''Acta Oto-Laryngologica''' is a peer-reviewed [[medical journal]] that focuses on the '''Acta Oto-Laryngologica''' publishes original research articles, review articles, and
    2 KB (261 words) - 22:31, 10 March 2024
  • '''Oto-Palatal-Digital Syndrome''' (OPD syndrome) is a rare genetic disorder that a The symptoms of Oto-Palatal-Digital Syndrome can vary widely among affected individuals but gene
    3 KB (425 words) - 20:54, 30 March 2024
  • ...divided into two main types: Oto-Palato-Digital Syndrome Type 1 (OPD1) and Oto-Palato-Digital Syndrome Type 2 (OPD2), each caused by mutations in the ''FLN ===Oto-Palato-Digital Syndrome Type 1===
    3 KB (498 words) - 02:19, 22 March 2024
  • 4 KB (583 words) - 01:30, 24 April 2024
  • 1 KB (152 words) - 03:54, 30 November 2021
  • ===European Federation of Oto-Rhino-Laryngological Societies (EUFOS)=== The [[European Federation of Oto-Rhino-Laryngological Societies]] (EUFOS) represents numerous national ENT so
    4 KB (498 words) - 15:35, 31 March 2024
  • ...n lead to [[congenital disorders]] such as [[Klippel-Feil syndrome]] and [[oto-facial syndrome]]. ...nes in the neck, which is caused by mutations in the PAX1 gene. Similarly, oto-facial syndrome, a condition characterized by ear and facial abnormalities,
    2 KB (272 words) - 05:53, 10 March 2024
  • 1 KB (115 words) - 19:44, 7 December 2021
  • 1 KB (115 words) - 21:46, 7 December 2021
  • 1 KB (115 words) - 22:34, 7 December 2021
  • 1 KB (115 words) - 22:31, 7 December 2021
  • 1 KB (140 words) - 22:32, 7 December 2021
  • 2 KB (279 words) - 19:03, 25 February 2024

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