Kim M. Keppler-Noreuil
Division of Medical Genetics
University of Iowa Children's Hospital
Iowa City
Iowa 52242
USA
Name/email consistency: high
- Binder phenotype: associated findings and etiologic mechanisms. Keppler-Noreuil, K.M., Wenzel, T.J. J. Craniofac. Surg (2010)
- Prenatal ascertainment of OEIS complex/cloacal exstrophy - 15 new cases and literature review. Keppler-Noreuil, K., Gorton, S., Foo, F., Yankowitz, J., Keegan, C. Am. J. Med. Genet. A (2007)
- Syndrome of congenital cataracts, sensorineural deafness, Down syndrome-like facial appearance, short stature, and mental retardation: two additional cases. Keppler-Noreuil, K., Welch, J., Baker-Lange, K. Am. J. Med. Genet. A (2007)
- Atypical Down syndrome phenotype with severe developmental delay, hypertonia, and seizures in a child with translocation trisomy 21. Keppler-Noreuil, K.M., Welch, J.L., Major, H.J., Qiau, Q., Jordan, D.K., Patil, S.R. Dev. Med. Child. Neurol (2002)
- OEIS complex (omphalocele-exstrophy-imperforate anus-spinal defects): a review of 14 cases. Keppler-Noreuil, K.M. Am. J. Med. Genet. (2001)
