Kristina Cusmano-Ozog

Summary

Affiliation: Stanford University
Country: USA

Publications

  1. ncbi 22q13.3 deletion syndrome: a recognizable malformation syndrome associated with marked speech and language delay
    Kristina Cusmano-Ozog
    Division of Medical Genetics, H 315, Department of Pediatrics, Stanford University School of Medicine, Stanford, CA 94305 5208, USA
    Am J Med Genet C Semin Med Genet 145:393-8. 2007
  2. ncbi Progressive and symmetric supraorbital hyperostosis with bony and soft tissue overgrowth in an Ethiopian female: a newly recognized overgrowth syndrome?
    Margaret P Adam
    Department of Human Genetics, Division of Medical Genetics, Emory University School of Medicine, Atlanta, Georgia 30030, USA
    Am J Med Genet A 146:543-7. 2008

Detail Information

Publications2

  1. ncbi 22q13.3 deletion syndrome: a recognizable malformation syndrome associated with marked speech and language delay
    Kristina Cusmano-Ozog
    Division of Medical Genetics, H 315, Department of Pediatrics, Stanford University School of Medicine, Stanford, CA 94305 5208, USA
    Am J Med Genet C Semin Med Genet 145:393-8. 2007
    ....
  2. ncbi Progressive and symmetric supraorbital hyperostosis with bony and soft tissue overgrowth in an Ethiopian female: a newly recognized overgrowth syndrome?
    Margaret P Adam
    Department of Human Genetics, Division of Medical Genetics, Emory University School of Medicine, Atlanta, Georgia 30030, USA
    Am J Med Genet A 146:543-7. 2008
    ..However, the bone began to regrow in a symmetric fashion within 3 months of removal. This patient's phenotype is at variance with any known overgrowth syndrome...