Tellier, A.L., Cormier-Daire, V., Abadie, V., Amiel, J., Sigaudy, S., Bonnet, D., de Lonlay-Debeney, P., Morrisseau-Durand, M.P., Hubert, P., Michel, J.L., Jan, D., Dollfus, H., Baumann, C., Labrune, P., Lacombe, D., Philip, N., LeMerrer, M., Briard, M.L., Munnich, A. and Lyonnet, S. (1998) CHARGE Syndrome: Report of 47 Cases and Review. American Journal of Medical Genetics, 76, 402-409.
http://dx.doi.org/10.1002/(SICI)1096-8628(19980413)76:5<402::AID-AJMG7>3.0.CO;2-O

has been cited by the following article:

• TITLE: Charge Syndrome—A Case Report

  AUTHORS: A. Ravindran, A. Amirthagani, Prince Peter Dhas, S. Nagarajan, Senthil Kumar, Satheesh Kumar,   Venkatesh

  KEYWORDS: Charge Syndrome, Choanal Atresia, Coloboma

  JOURNAL NAME: International Journal of Otolaryngology and Head & Neck Surgery, Vol.4 No.2, March 24, 2015

  ABSTRACT: CHARGE syndrome is a rare, recently well recognized entity with non-random pattern of congenital anomalies. The syndrome associations consist of C-coloboma of the eyes, H-heart disease, A-atresia of the choanae, R-retarded growth and development, G-genital hypoplasia/genitourinary anomalies and E-ear anomalies and/or hearing loss. All anomalies are not seen in every case and a varied spectrum of associations is seen in most of the cases. The exact incidence is not known. However, the reported prevalence is approximately 1:10,000 births. We report one such case.