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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Kim M. Keppler-Noreuil

Division of Medical Genetics

University of Iowa Children's Hospital

Iowa City

Iowa 52242



Name/email consistency: high



  • Division of Medical Genetics, University of Iowa Children's Hospital, Iowa City, Iowa 52242, USA. 2001 - 2010
  • University of Iowa Hospitals and Clinics, Department of Pediatrics, Iowa City 52232, USA. 2002


  1. Binder phenotype: associated findings and etiologic mechanisms. Keppler-Noreuil, K.M., Wenzel, T.J. J. Craniofac. Surg (2010) [Pubmed]
  2. 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) [Pubmed]
  3. 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) [Pubmed]
  4. 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) [Pubmed]
  5. OEIS complex (omphalocele-exstrophy-imperforate anus-spinal defects): a review of 14 cases. Keppler-Noreuil, K.M. Am. J. Med. Genet. (2001) [Pubmed]
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