S Spranger

Summary

Country: Germany

Publications

  1. ncbi request reprint Léri-Weill syndrome as part of a contiguous gene syndrome at Xp22.3
    S Spranger
    Center for Human Genetics and Genetic Counseling, University of Bremen, Germany
    Am J Med Genet 83:367-71. 1999
  2. ncbi request reprint Interstitial deletion of 5q33.3q35.1 in a girl with mild mental retardation
    S Spranger
    Center for Human Genetics and Genetic Counselling, University of Bremen, Germany
    Am J Med Genet 93:107-9. 2000

Collaborators

Detail Information

Publications2

  1. ncbi request reprint Léri-Weill syndrome as part of a contiguous gene syndrome at Xp22.3
    S Spranger
    Center for Human Genetics and Genetic Counseling, University of Bremen, Germany
    Am J Med Genet 83:367-71. 1999
    ..We discuss the phenotype in relationship to hitherto published cases with chromosomal aberrations and contiguous gene syndromes of Xp22.3...
  2. ncbi request reprint Interstitial deletion of 5q33.3q35.1 in a girl with mild mental retardation
    S Spranger
    Center for Human Genetics and Genetic Counselling, University of Bremen, Germany
    Am J Med Genet 93:107-9. 2000
    ..But severe mental retardation seems to be a consistent manifestation. We describe a 4-year-old girl with a de novo deletion of 5q33.3q35.1 presenting only with mild psychomotor delay, minor facial anomalies, and seizures...