A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome

Mark J. Rieder, Glenn E. Green, Sarah S. Park, Brendan D. Stamper, Christopher T. Gordon, Jason M. Johnson, Christopher M. Cunniff, Joshua D. Smith, Sarah B. Emery, Stanislas Lyonnet, Jeanne Amiel, Muriel Holder, Andrew A. Heggie, Michael J. Bamshad, Deborah A. Nickerson, Timothy C. Cox, Anne V. Hing, Jeremy A. Horst, Michael L. Cunningham

Research output: Contribution to journalComment/debate

Original languageEnglish (US)
Number of pages1
JournalAmerican Journal of Human Genetics
Volume91
Issue number2
DOIs
StatePublished - Aug 10 2012

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Rieder, M. J., Green, G. E., Park, S. S., Stamper, B. D., Gordon, C. T., Johnson, J. M., Cunniff, C. M., Smith, J. D., Emery, S. B., Lyonnet, S., Amiel, J., Holder, M., Heggie, A. A., Bamshad, M. J., Nickerson, D. A., Cox, T. C., Hing, A. V., Horst, J. A., & Cunningham, M. L. (2012). A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome. American Journal of Human Genetics, 91(2). https://doi.org/10.1016/j.ajhg.2012.07.011