Jakobsen, L.P., Ullmann, R., Christensen, S.B., et al. (2007) Pierre Robin Sequence May Be Caused by Dysregulation of SOX9 and KCNJ2. Journal of Medical Genetics, 44, 381-386.
http://dx.doi.org/10.1136/jmg.2006.046177

has been cited by the following article:

• TITLE: A Pierre Robin Syndrome with Absent Anterior 2/3 Tongue—A Case Report

  AUTHORS: K. Surender, K. Vasudev, B. Balaram, C. H. Vijay Raj, Lingaiah Jadi

  KEYWORDS: Micrognathia, Glossoptosis, Pierre Robin Sequence

  JOURNAL NAME: International Journal of Otolaryngology and Head & Neck Surgery, Vol.4 No.6, November 23, 2015

  ABSTRACT: The triad of micrognathia, glossoptosis and airway obstruction originally described in 1923 by Pierre Robin, is known as Robin sequence (or Pierre robin sequence “PRS”). PRS is characterized by micrognathia (small and symmetrical receded mandible), glossoptosis (tongue of variable size falls backwards into the post pharyngeal wall), and cleft palate (U or V shaped). We report a case of 2 hours old newborn presented with micrognathia, retrognathia, and glossoptosis and absent anterior two thirds of tongue.